Version 4.0.201701

Home - Cell Index - Search - Web Sites
Species - Tissues - Tumors - Pathologies - Tr. Agents
Collections - Laboratories - Catalogues

For information, get in touch with: Dott.ssa Barbara Parodi
Email: barbara.parodi@hsanmartino.it
  P. Romano, A. Manniello et al. Nucl Acids Res 2009 37:D925-D932.
DOI: doi:10.1093/nar/gkn730; PMID: 18927105

Short description of cell lines
Tissue/organ: skin, fibroblast


- By clicking on the cell line name, you will retrieve the detailed description of the cell line
- By clicking on one of the terms between parentheses, you will retrieve the list of all relevant cell lines

1184 (human) - ECACC
1221 (human) - ECACC
1306 (human) - ECACC
142BR (human) - ECACC
149BR (human) - ECACC
153BR (human) - ECACC
155BR (human) - ECACC
161BR (human) - ECACC
162 (human, Caucasian) - BGEBS
163 (human, Caucasian) - BGEBS
171BR (human) - ECACC
174BR (human) - ECACC
175BR (human) - ECACC
180BR (human) - ECACC
1BR.3.G (human) - ECACC
1BR.3.GN (human) - ECACC
1BR.3.N (human) - ECACC
1BR3 (human) - ECACC
46Br.1G1 (human) - ECACC
84BR (human) - ECACC
AG 5025 (human, Caucasian) - BGEBS
Amdur II (human, Caucasian, methylmalonicacidemia) - ECACC
Amdur II (human, Caucasian, methylmalonicacidemia) - IZSBS
B/C.Sk (mouse) - ECACC
BUD-8 (human, Caucasian) - ECACC
BUD-8 (human, Caucasian) - IZSBS
C1PV (human, Caucasian) - PVCGU
C2PV (human, Caucasian) - PVCGU
C3PV (human, Caucasian) - PVCGU
C4PV (human, Caucasian) - PVCGU
C5PV (human, Caucasian) - PVCGU
C6PV (human, Caucasian, porokeratosis of Mibelli) - PVCGU
C7PV (human, Caucasian, photosensitivity) - PVCGU
C8PV (human, Caucasian) - PVCGU
C9PV (human, Caucasian) - PVCGU
CHP 3 (human, Black, galactosemia) - IZSBS
CHP 4 (human, Black, asymptomatic galactosemia) - IZSBS
Cor Per (human, Caucasian, Ehlers-Danlos syndrome, type IV, autosomal dominant) - BGEBS
Cri du Chat (human, Caucasian, cri du chat syndrome) - ECACC
CS1PV (human, Caucasian, Cockayne syndrome) - PVCGU
Da Mo (human, Caucasian, Ehlers-Danlos syndrome, type V) - BGEBS
Detroit 510 (human, Caucasian, galactosemia) - ECACC
Detroit 510 (human, Caucasian, galactosemia) - IZSBS
Detroit 525 (human, Caucasian, Turner syndrome/noonan syndrome 1) - ECACC
Detroit 525 (human, Caucasian, Turner syndrome/noonan syndrome 1) - IZSBS
Detroit 529 (human, Caucasian, trisomy 21 / Down syndrome) - ECACC
Detroit 529 (human, Caucasian, trisomy 21 / Down syndrome) - IZSBS
Detroit 539 (human, Caucasian, trisomy 21 / Down syndrome) - ECACC
Detroit 539 (human, Caucasian, trisomy 21 / Down syndrome) - IZSBS
Detroit 548 (human, Caucasian, partial D trisomy) - IZSBS
Detroit 550 (human) - IZSBS
Detroit 573 (human, Caucasian, B/D translocation) - ECACC
Detroit 573 (human, Caucasian, B/D translocation) - IZSBS
DSH1PV (human, Caucasian, dyschromatosis symmetrica hereditaria) - PVCGU
DSH2PV (human, Caucasian, dyschromatosis symmetrica hereditaria) - PVCGU
DSH3PV (human, Caucasian, dyschromatosis symmetrica hereditaria) - PVCGU
DSH4PV (human, Caucasian, dyschromatosis symmetrica hereditaria) - PVCGU
EDS 100 (human, Caucasian, Ehlers-Danlos syndrome, type III) - BGEBS
EDS 101 (human, Caucasian, Ehlers-Danlos syndrome, type III) - BGEBS
EDS 105 (human, Caucasian, Ehlers-Danlos syndrome, type VII) - BGEBS
Fer Ray (human, Caucasian, Ehlers-Danlos syndrome, type VIII) - BGEBS
FG/223 (rat, Galliera) - SSUFG
FG/25 (rat, Galliera) - SSUFG
FG/4 (rat, Galliera) - SSUFG
FG/45 (rat, Galliera) - SSUFG
FG/90 (rat, Galliera) - SSUFG
FH 1 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 10 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 100 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 101 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 103 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 105 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 106 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 111 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 112 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 113 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 114 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 118 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 119 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 120 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 121 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 124 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 125 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 126 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 129 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 13 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 130 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 131 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 132 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 133 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 134 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 135 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 136 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 137 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 138 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 14 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 140 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 141 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 142 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 143 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 144 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 145 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 146 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 147 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 148 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 149 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 15 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 150 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 151 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 152 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 153 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 154 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 155 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 156 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 157 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 16 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 160 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 161 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 162 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 163 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 164 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 165 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 167 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 168 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 169 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 17 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 170 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 171 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 172 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 176 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 177 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 178 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 18 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 19 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 20 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 21 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 22 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 23 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 24 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 25 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 26 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 27 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 29 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 30 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 31 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 32 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 33 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 34 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 35 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 36 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 37 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 38 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 39 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 4 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 47 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 49 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 5 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 50 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 51 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 52 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 53 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 54 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 55 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 56 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 57 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 59 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 6 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 60 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 61 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 62 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 63 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 64 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 65 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 66 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 67 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 68 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 69 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 7 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 70 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 71 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 72 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 73 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 74 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 75 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 76 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 77 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 78 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 79 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 8 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 80 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 81 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 82 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 83 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 84 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 85 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 86 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 9 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 91 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 92 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 93 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 94 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 95 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 96 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 97 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 98 (human, Caucasian, hypercholesterolemia, familial) - DSB
FH 99 (human, Caucasian, hypercholesterolemia, familial) - DSB
FIB-CL1 (human, Caucasian, cutis laxa, recessive, type I) - DSB
FIB-CL10 (human, Caucasian, cutis laxa, recessive, type I) - DSB
FIB-CL2 (human, Caucasian, cutis laxa, recessive, type I) - DSB
FIB-CL3 (human, Caucasian, cutis laxa, recessive, type I) - DSB
FIB-CL5 (human, Caucasian, cutis laxa, recessive, type I) - DSB
FIB-CL6 (human, Caucasian, cutis laxa, recessive, type I) - DSB
FIB-CL7 (human, Caucasian, cutis laxa, recessive, type I) - DSB
FIB-CL8 (human, Caucasian, cutis laxa, recessive, type I) - DSB
FIB-CL9 (human, Caucasian, cutis laxa, recessive, type I) - DSB
FIB-DUP1 (human, Caucasian, Dupuytren contracture) - DSB
FIB-DUP10 (human, Caucasian, Dupuytren contracture) - DSB
FIB-DUP11 (human, Caucasian, Dupuytren contracture) - DSB
FIB-DUP14 (human, Caucasian, Dupuytren contracture) - DSB
FIB-DUP15 (human, Caucasian, Dupuytren contracture) - DSB
FIB-DUP3 (human, Caucasian, Dupuytren contracture) - DSB
FIB-DUP4 (human, Caucasian, Dupuytren contracture) - DSB
FIB-DUP5 (human, Caucasian, Dupuytren contracture) - DSB
FIB-DUP6 (human, Caucasian, Dupuytren contracture) - DSB
FIB-DUP7 (human, Caucasian, Dupuytren contracture) - DSB
FIB-DUP9 (human, Caucasian, Dupuytren contracture) - DSB
FIB-EDII1 (human, Caucasian, Ehlers-Danlos syndrome) - DSB
FIB-EDII11 (human, Caucasian, Ehlers-Danlos syndrome) - DSB
FIB-EDIII5 (human, Caucasian, Ehlers-Danlos syndrome) - DSB
FIB-EDIV2 (human, Caucasian, Ehlers-Danlos syndrome) - DSB
FIB-EDIV4 (human, Caucasian, Ehlers-Danlos syndrome) - DSB
FIB-IP1 (human, Caucasian, cutaneous hyperlaxity) - DSB
FIB-IP2 (human, Caucasian, cutaneous hyperlaxity) - DSB
FIB-LARSEN1 (human, Caucasian, Larsen syndrome) - DSB
FIB-LARSEN2 (human, Caucasian, Larsen syndrome) - DSB
FIB-MARFAN1 (human, Caucasian, Marfan syndrome) - DSB
FIB-MARFAN3 (human, Caucasian, Marfan syndrome) - DSB
FIB-MARFAN4 (human, Caucasian, Marfan syndrome) - DSB
FIB-MARFAN5 (human, Caucasian, Marfan syndrome) - DSB
FIB-MARFAN6 (human, Caucasian, Marfan syndrome) - DSB
FIB-MOR1 (human, Caucasian, mucopolysaccharidosis type IV B / Morquio syndrome) - DSB
FIB-NC15 (human, Caucasian) - DSB
FIB-NC16 (human, Caucasian) - DSB
FIB-NC23 (human, Caucasian) - DSB
FIB-NC25 (human, Caucasian) - DSB
FIB-NC27 (human, Caucasian) - DSB
FIB-NC30 (human, Caucasian) - DSB
FIB-NC42 (human, Caucasian) - DSB
FIB-NC46 (human, Caucasian) - DSB
FIB-NC54 (human, Caucasian) - DSB
FIB-NC55 (human, Caucasian) - DSB
FIB-NC56 (human, Caucasian) - DSB
FIB-NC57 (human, Caucasian) - DSB
FIB-NC58 (human, Caucasian) - DSB
FIB-NC59 (human, Caucasian) - DSB
FIB-NC60 (human, Caucasian) - DSB
FIB-NC62 (human, Caucasian) - DSB
FIB-NC63 (human, Caucasian) - DSB
FIB-NC64 (human, Caucasian) - DSB
FIB-NC65 (human, Caucasian) - DSB
FIB-NC66 (human, Caucasian) - DSB
FIB-NC67 (human, Caucasian) - DSB
FIB-PROL1 (human, Caucasian, prolidase deficiency) - DSB
FIB-PROL2 (human, Caucasian, prolidase deficiency) - DSB
FIB-PSE1 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE12 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE13 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE14 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE15 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE17 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE2 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE26 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE3 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE32 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE34 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE35 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE39 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE40 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE43 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE44 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE45 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE46 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE47 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE50 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE51 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE52 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE53 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-PSE54 (human, Caucasian, pseudoxanthoma elasticum) - DSB
FIB-SCLE1 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE10 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE11 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE12 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE13 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE14 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE15 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE16 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE17 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE18 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE19 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE2 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE20 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE21 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE3 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE4 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE5 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE6 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE7 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE8 (human, Caucasian, scleroderma, familial progressive) - DSB
FIB-SCLE9 (human, Caucasian, scleroderma, familial progressive) - DSB
GA87 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
GM00425 (human) - BGEBS
GM00637B (human, Caucasian) - NAUBC
GM01229 (human) - BGEBS
GM02185 (human, Caucasian) - GEIMG
GM02290 (human, Caucasian, Lesch-Nyhan syndrome) - MIISA
GM02848 (human, Caucasian) - BGEBS
GP-16 (human, pyroglutamicaciduria / 5-oxoprolinuria) - RMSTC
GS-109-V-20 (human, Caucasian, Gardner's syndrome) - ECACC
GS-109-V-34 (human, Caucasian, Gardner's syndrome) - ECACC
GS-109-V-63 (human, Caucasian, Gardner's syndrome) - ECACC
HEL (human, Caucasian) - GEIMM
HG 261 (human, Caucasian, Fanconi anemia) - IZSBS
HG261 (human, Caucasian, Fanconi anemia) - ECACC
HSF (human) - MIECC
HSFPD (human, Parkinson disease) - MIECC
IGF001/00 (human, Caucasian) - GEIMM
IGF001/01 (human, Caucasian) - GEIMM
IGF001/77 (human, Caucasian) - GEIMM
IGF001/78 (human, Caucasian, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF001/80 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF001/81 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF001/83 (human, Caucasian) - GEIMM
IGF001/84 (human, Caucasian) - GEIMM
IGF001/85 (human, Caucasian) - GEIMM
IGF001/86 (human, Caucasian) - GEIMM
IGF001/87 (human, Caucasian) - GEIMM
IGF001/90 (human, Caucasian, Steinert disease) - GEIMM
IGF001/91 (human, Caucasian, Charcot-Marie-Tooth disease) - GEIMM
IGF001/93 (human, Caucasian) - GEIMM
IGF001/94 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF001/95 (human, Caucasian) - GEIMM
IGF001/96 (human, Caucasian, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF001/97 (human, Caucasian) - GEIMM
IGF001/98 (human, Caucasian, Glutaricacidemia I) - GEIMM
IGF001/99 (human, Caucasian) - GEIMM
IGF002/00 (human, Caucasian, Krabbe disease) - GEIMM
IGF002/01 (human, Caucasian) - GEIMM
IGF002/77 (human, Caucasian) - GEIMM
IGF002/78 (human, Caucasian, phenylketonuria II) - GEIMM
IGF002/79 (human, Caucasian) - GEIMM
IGF002/80 (human, Caucasian, Fanconi-Bickel syndrome) - GEIMM
IGF002/81 (human, Caucasian) - GEIMM
IGF002/82 (human, Caucasian) - GEIMM
IGF002/83 (human, Caucasian) - GEIMM
IGF002/85 (human, Caucasian, osteogenesis imperfecta) - GEIMM
IGF002/86 (human, Caucasian) - GEIMM
IGF002/87 (human, Caucasian) - GEIMM
IGF002/88 (human, Caucasian, propionicacidemia I) - GEIMM
IGF002/90 (human, Caucasian) - GEIMM
IGF002/91 (human, Caucasian) - GEIMM
IGF002/92 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF002/93 (human, Caucasian) - GEIMM
IGF002/94 (human, Caucasian) - GEIMM
IGF002/95 (human, Caucasian, McCune-Albright sindrome) - GEIMM
IGF002/96 (human, Caucasian, DiGeorge syndrome) - GEIMM
IGF002/97 (human, Caucasian) - GEIMM
IGF002/98 (human, Caucasian) - GEIMM
IGF002/99 (human, Caucasian) - GEIMM
IGF003/00 (human, Caucasian) - GEIMM
IGF003/01 (human, Caucasian) - GEIMM
IGF003/77 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF003/80 (human, Caucasian) - GEIMM
IGF003/81 (human, Caucasian) - GEIMM
IGF003/82 (human, Caucasian, metatropic dwarfism, type II) - GEIMM
IGF003/83 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF003/85 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF003/86 (human, Caucasian) - GEIMM
IGF003/87 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF003/88 (human, Caucasian) - GEIMM
IGF003/89 (human, Caucasian, Freeman-Sheldon syndrome) - GEIMM
IGF003/92 (human, South American, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF003/93 (human, Caucasian) - GEIMM
IGF003/94 (human, Caucasian) - GEIMM
IGF003/96 (human, Caucasian) - GEIMM
IGF003/97 (human, Caucasian) - GEIMM
IGF003/98 (human, Caucasian) - GEIMM
IGF003/99 (human, Caucasian) - GEIMM
IGF004/00 (human, Caucasian, salla disease) - GEIMM
IGF004/01 (human, Caucasian) - GEIMM
IGF004/78 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF004/79 (human, Caucasian) - GEIMM
IGF004/81 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF004/82 (human, Caucasian) - GEIMM
IGF004/83 (human, Caucasian) - GEIMM
IGF004/84 (human, Caucasian, methylmalonicacidemia) - GEIMM
IGF004/85 (human, Caucasian, Menkes syndrome) - GEIMM
IGF004/86 (human, Caucasian) - GEIMM
IGF004/87 (human, Caucasian) - GEIMM
IGF004/89 (human, Caucasian, metatropic dwarfism, type II) - GEIMM
IGF004/91 (human, Caucasian, Ehlers-Danlos syndrome, type IV, autosomal dominant) - GEIMM
IGF004/93 (human, Caucasian) - GEIMM
IGF004/94 (human, Caucasian) - GEIMM
IGF004/96 (human, Caucasian, Cockayne syndrome) - GEIMM
IGF004/97 (human, Caucasian) - GEIMM
IGF004/98 (human, Caucasian, neuropathy, giant axonal) - GEIMM
IGF004/99 (human, Caucasian) - GEIMM
IGF005/00 (human, Caucasian) - GEIMM
IGF005/01 (human, Caucasian) - GEIMM
IGF005/77 (human, Caucasian) - GEIMM
IGF005/80 (human, Caucasian) - GEIMM
IGF005/82 (human, Caucasian) - GEIMM
IGF005/83 (human, Caucasian) - GEIMM
IGF005/84 (human, Caucasian, methylmalonicacidemia) - GEIMM
IGF005/85 (human, Caucasian) - GEIMM
IGF005/86 (human, Caucasian) - GEIMM
IGF005/87 (human, Caucasian) - GEIMM
IGF005/89 (human, Caucasian) - GEIMM
IGF005/91 (human, Caucasian) - GEIMM
IGF005/92 (human, Caucasian, NARP mutation) - GEIMM
IGF005/93 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF005/94 (human, Caucasian) - GEIMM
IGF005/95 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF005/96 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF005/97 (human, Caucasian) - GEIMM
IGF005/98 (human, Caucasian, glycogen storage disease IV) - GEIMM
IGF005/99 (human, Caucasian) - GEIMM
IGF006/00 (human, Caucasian) - GEIMM
IGF006/01 (human, Caucasian) - GEIMM
IGF006/77 (human, Caucasian) - GEIMM
IGF006/79 (human, Caucasian) - GEIMM
IGF006/80 (human, Caucasian, camptomelic dwarfism) - GEIMM
IGF006/81 (human, Caucasian) - GEIMM
IGF006/82 (human, Caucasian, hypophosphatasia infantile) - GEIMM
IGF006/83 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF006/84 (human, Caucasian, mucolipidosis II) - GEIMM
IGF006/85 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF006/86 (human, Caucasian) - GEIMM
IGF006/87 (human, Caucasian) - GEIMM
IGF006/89 (human, Caucasian) - GEIMM
IGF006/91 (human, Caucasian) - GEIMM
IGF006/92 (human, Caucasian, neuraminidase deficiency) - GEIMM
IGF006/93 (human, Caucasian, homocystinuria - megaloblastic anemia) - GEIMM
IGF006/94 (human, Caucasian, neuraminidase deficiency with beta-galactosidase deficiency) - GEIMM
IGF006/95 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF006/96 (human, Caucasian) - GEIMM
IGF006/97 (human, Caucasian) - GEIMM
IGF006/98 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF006/99 (human, Caucasian) - GEIMM
IGF007/00 (human, Caucasian) - GEIMM
IGF007/01 (human, Caucasian) - GEIMM
IGF007/79 (human, Caucasian) - GEIMM
IGF007/80 (human, Caucasian) - GEIMM
IGF007/81 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF007/84 (human, Caucasian) - GEIMM
IGF007/85 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF007/86 (human, Caucasian) - GEIMM
IGF007/87 (human, Caucasian) - GEIMM
IGF007/89 (human, Caucasian, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF007/90 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF007/91 (human, Caucasian) - GEIMM
IGF007/92 (human, Caucasian, Cockayne syndrome) - GEIMM
IGF007/93 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF007/95 (human, Caucasian) - GEIMM
IGF007/96 (human, Caucasian) - GEIMM
IGF007/97 (human, Caucasian) - GEIMM
IGF007/98 (human, Caucasian, Davidson disease) - GEIMM
IGF007/99 (human, Caucasian) - GEIMM
IGF008/00 (human, Caucasian) - GEIMM
IGF008/01 (human, Caucasian) - GEIMM
IGF008/78 (human, Caucasian) - GEIMM
IGF008/79 (human, Caucasian) - GEIMM
IGF008/80 (human, Caucasian, neuraminidase deficiency) - GEIMM
IGF008/81 (human, Caucasian) - GEIMM
IGF008/82 (human, Caucasian, Gaucher disease type III) - GEIMM
IGF008/84 (human, Caucasian, mucopolysaccharidosis type III C) - GEIMM
IGF008/86 (human, Caucasian) - GEIMM
IGF008/87 (human, Caucasian) - GEIMM
IGF008/88 (human, Caucasian) - GEIMM
IGF008/89 (human, Caucasian, osteogenesis imperfecta, type II) - GEIMM
IGF008/92 (human, Caucasian) - GEIMM
IGF008/94 (human, Caucasian) - GEIMM
IGF008/96 (human, Caucasian) - GEIMM
IGF008/97 (human, Caucasian) - GEIMM
IGF008/98 (human, Caucasian) - GEIMM
IGF008/99 (human, Caucasian) - GEIMM
IGF009/00 (human, Caucasian) - GEIMM
IGF009/01 (human, Caucasian) - GEIMM
IGF009/77 (human, Caucasian, Gaucher disease type III) - GEIMM
IGF009/78 (human, Caucasian) - GEIMM
IGF009/80 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF009/81 (human, Caucasian, neuronal ceroid-lipofuscinosis infantile Finnish type) - GEIMM
IGF009/82 (human, Caucasian) - GEIMM
IGF009/84 (human, Caucasian, neuraminidase deficiency) - GEIMM
IGF009/85 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF009/86 (human, Caucasian, mucopolysaccharidosis type III C) - GEIMM
IGF009/87 (human, Caucasian) - GEIMM
IGF009/88 (human, Caucasian) - GEIMM
IGF009/89 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF009/90 (human, Caucasian, Zellweger syndrome) - GEIMM
IGF009/91 (human, Caucasian) - GEIMM
IGF009/92 (human, Caucasian) - GEIMM
IGF009/93 (human, Caucasian, Krabbe disease) - GEIMM
IGF009/94 (human, Caucasian) - GEIMM
IGF009/96 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF009/97 (human, Caucasian) - GEIMM
IGF009/98 (human, Caucasian, Pallister Killian syndrome) - GEIMM
IGF009/99 (human, Caucasian) - GEIMM
IGF010/00 (human, Caucasian) - GEIMM
IGF010/77 (human, Caucasian, Sandhoff disease) - GEIMM
IGF010/78 (human, Caucasian) - GEIMM
IGF010/80 (human, Caucasian) - GEIMM
IGF010/81 (human, Caucasian, mucolipidosis II) - GEIMM
IGF010/83 (human, Caucasian) - GEIMM
IGF010/84 (human, Caucasian, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF010/85 (human, Caucasian) - GEIMM
IGF010/86 (human, Caucasian) - GEIMM
IGF010/87 (human, Caucasian) - GEIMM
IGF010/88 (human, Caucasian) - GEIMM
IGF010/89 (human, Caucasian) - GEIMM
IGF010/90 (human, Caucasian, Wilson disease) - GEIMM
IGF010/91 (human, Caucasian) - GEIMM
IGF010/92 (human, Caucasian) - GEIMM
IGF010/93 (human, Caucasian) - GEIMM
IGF010/94 (human, Caucasian, Marfan syndrome) - GEIMM
IGF010/96 (human, Caucasian, mucolipidosis II) - GEIMM
IGF010/97 (human, Caucasian) - GEIMM
IGF010/98 (human, Caucasian) - GEIMM
IGF010/99 (human, Caucasian) - GEIMM
IGF011/00 (human, Caucasian) - GEIMM
IGF011/01 (human, Caucasian) - GEIMM
IGF011/77 (human, Caucasian, Ehlers-Danlos syndrome, type I) - GEIMM
IGF011/78 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF011/80 (human, Caucasian) - GEIMM
IGF011/81 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF011/82 (human, Caucasian, amaurotic family idiocy, juvenile type/neuronal ceroid lipofuscinosis) - GEIMM
IGF011/83 (human, Caucasian) - GEIMM
IGF011/84 (human, Caucasian) - GEIMM
IGF011/85 (human, Caucasian) - GEIMM
IGF011/86 (human, Caucasian) - GEIMM
IGF011/87 (human, Caucasian) - GEIMM
IGF011/89 (human, Caucasian) - GEIMM
IGF011/90 (human, Caucasian) - GEIMM
IGF011/91 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF011/92 (human, Caucasian, Ehlers-Danlos syndrome, type I) - GEIMM
IGF011/93 (human, Caucasian) - GEIMM
IGF011/94 (human, Caucasian) - GEIMM
IGF011/96 (human, Caucasian, homocystinuria - megaloblastic anemia) - GEIMM
IGF011/97 (human, Caucasian) - GEIMM
IGF011/98 (human, Caucasian) - GEIMM
IGF011/99 (human, Caucasian, osteopetrosis autosomal recessive) - GEIMM
IGF012/00 (human, Caucasian) - GEIMM
IGF012/01 (human, Caucasian) - GEIMM
IGF012/77 (human, Caucasian) - GEIMM
IGF012/78 (human, Caucasian) - GEIMM
IGF012/80 (human, Caucasian) - GEIMM
IGF012/81 (human, Caucasian, tyrosine transaminase deficiency) - GEIMM
IGF012/82 (human, Caucasian) - GEIMM
IGF012/83 (human, Caucasian) - GEIMM
IGF012/84 (human, Caucasian) - GEIMM
IGF012/85 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF012/86 (human, Caucasian) - GEIMM
IGF012/87 (human, Caucasian, spondyloepiphyseal dysplasia, congenital) - GEIMM
IGF012/89 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF012/90 (human, Caucasian, hydrocephalus, agyria, retinal dysplasia Hard syndrome/Walker-Warburg) - GEIMM
IGF012/91 (human, Caucasian, Krabbe disease) - GEIMM
IGF012/92 (human, Caucasian) - GEIMM
IGF012/93 (human, Caucasian) - GEIMM
IGF012/94 (human, Caucasian) - GEIMM
IGF012/96 (human, Caucasian) - GEIMM
IGF012/98 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF012/99 (human, Caucasian, Austin) - GEIMM
IGF013/00 (human, Caucasian) - GEIMM
IGF013/01 (human, Caucasian) - GEIMM
IGF013/77 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF013/78 (human, Caucasian) - GEIMM
IGF013/80 (human, Caucasian) - GEIMM
IGF013/81 (human, Caucasian, tyrosine transaminase deficiency) - GEIMM
IGF013/82 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF013/84 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF013/85 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF013/86 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF013/87 (human, Caucasian) - GEIMM
IGF013/89 (human, Caucasian) - GEIMM
IGF013/90 (human, Caucasian, mucolipidosis II) - GEIMM
IGF013/91 (human, Caucasian) - GEIMM
IGF013/92 (human, Caucasian) - GEIMM
IGF013/93 (human, Caucasian) - GEIMM
IGF013/94 (human, Caucasian) - GEIMM
IGF013/95 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF013/96 (human, Caucasian) - GEIMM
IGF013/99 (human, Caucasian, sulfatidosis, juvenile, Austin type) - GEIMM
IGF014/00 (human, Caucasian) - GEIMM
IGF014/01 (human, Caucasian) - GEIMM
IGF014/78 (human, Caucasian) - GEIMM
IGF014/80 (human, Caucasian) - GEIMM
IGF014/81 (human, Caucasian) - GEIMM
IGF014/82 (human, Caucasian) - GEIMM
IGF014/83 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF014/84 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF014/85 (human, Caucasian) - GEIMM
IGF014/86 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF014/87 (human, Caucasian) - GEIMM
IGF014/89 (human, Caucasian, Menkes syndrome) - GEIMM
IGF014/90 (human, Caucasian, osteoporosis-pseudoglioma syndrome) - GEIMM
IGF014/91 (human, Caucasian, Lesch-Nyhan syndrome) - GEIMM
IGF014/92 (human, Caucasian) - GEIMM
IGF014/93 (human, Caucasian) - GEIMM
IGF014/94 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF014/95 (human, Caucasian) - GEIMM
IGF014/96 (human, Caucasian) - GEIMM
IGF014/97 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF014/98 (human, Caucasian) - GEIMM
IGF014/99 (human, Caucasian) - GEIMM
IGF015/00 (human, Caucasian) - GEIMM
IGF015/01 (human, Caucasian) - GEIMM
IGF015/78 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF015/80 (human, Caucasian) - GEIMM
IGF015/82 (human, Caucasian) - GEIMM
IGF015/83 (human, Caucasian) - GEIMM
IGF015/84 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF015/85 (human, Caucasian) - GEIMM
IGF015/86 (human, Caucasian) - GEIMM
IGF015/87 (human, Caucasian) - GEIMM
IGF015/90 (human, Caucasian, osteoporosis-pseudoglioma syndrome) - GEIMM
IGF015/91 (human, Caucasian) - GEIMM
IGF015/94 (human, Caucasian) - GEIMM
IGF015/95 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF015/96 (human, Caucasian, osteogenesis imperfecta) - GEIMM
IGF015/97 (human, Caucasian, def. PDH complex thiamine responsive) - GEIMM
IGF015/98 (human, Caucasian) - GEIMM
IGF015/99 (human, Caucasian) - GEIMM
IGF016/00 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF016/01 (human, Caucasian) - GEIMM
IGF016/77 (human, Caucasian, cystic fibrosis) - GEIMM
IGF016/78 (human, Caucasian, Ehlers-Danlos syndrome) - GEIMM
IGF016/80 (human, Caucasian) - GEIMM
IGF016/81 (human, Caucasian) - GEIMM
IGF016/82 (human, Caucasian, tyrosine transaminase deficiency) - GEIMM
IGF016/83 (human, Caucasian, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF016/84 (human, Caucasian) - GEIMM
IGF016/85 (human, Caucasian) - GEIMM
IGF016/86 (human, Caucasian, Marinesco-Sjogren syndrome) - GEIMM
IGF016/87 (human, Caucasian, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF016/89 (human, Caucasian) - GEIMM
IGF016/90 (human, Caucasian) - GEIMM
IGF016/91 (human, Caucasian) - GEIMM
IGF016/92 (human, Caucasian) - GEIMM
IGF016/93 (human, Caucasian) - GEIMM
IGF016/94 (human, Caucasian) - GEIMM
IGF016/95 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF016/96 (human, Caucasian, Krabbe disease) - GEIMM
IGF016/97 (human, Caucasian) - GEIMM
IGF016/98 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF016/99 (human, Caucasian) - GEIMM
IGF017/00 (human, Caucasian, mucopolysaccharidosis type III D) - GEIMM
IGF017/01 (human, Caucasian) - GEIMM
IGF017/76 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF017/78 (human, Caucasian, gangliosidosis, generalized GM1, type II) - GEIMM
IGF017/80 (human, Caucasian) - GEIMM
IGF017/82 (human, Caucasian, tyrosine transaminase deficiency) - GEIMM
IGF017/83 (human, Caucasian) - GEIMM
IGF017/84 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF017/85 (human, Caucasian) - GEIMM
IGF017/86 (human, Caucasian) - GEIMM
IGF017/87 (human, Caucasian) - GEIMM
IGF017/89 (human, Caucasian) - GEIMM
IGF017/90 (human, Caucasian, osteogenesis imperfecta, type II) - GEIMM
IGF017/91 (human, Caucasian) - GEIMM
IGF017/92 (human, Caucasian, Costello syndrome) - GEIMM
IGF017/93 (human, Caucasian) - GEIMM
IGF017/95 (human, Caucasian, leukoencephalopathy with vanishing white matter) - GEIMM
IGF017/96 (human, Caucasian) - GEIMM
IGF017/97 (human, Caucasian) - GEIMM
IGF017/98 (human, Caucasian) - GEIMM
IGF017/99 (human, Caucasian) - GEIMM
IGF018/00 (human, Caucasian, X duplication) - GEIMM
IGF018/01 (human, Caucasian) - GEIMM
IGF018/77 (human, Caucasian, mucopolysaccharidosis type III D) - GEIMM
IGF018/78 (human, Caucasian, Sandhoff disease) - GEIMM
IGF018/80 (human, Caucasian) - GEIMM
IGF018/81 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF018/82 (human, Caucasian) - GEIMM
IGF018/83 (human, Caucasian, Sandhoff disease) - GEIMM
IGF018/84 (human, Caucasian) - GEIMM
IGF018/85 (human, Caucasian, Gaucher disease type II) - GEIMM
IGF018/86 (human, Caucasian) - GEIMM
IGF018/87 (human, Caucasian) - GEIMM
IGF018/88 (human, Caucasian) - GEIMM
IGF018/89 (human, Caucasian) - GEIMM
IGF018/90 (human, Caucasian, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF018/91 (human, Caucasian) - GEIMM
IGF018/92 (human, Caucasian) - GEIMM
IGF018/93 (human, Caucasian, osteogenesis imperfecta, type II) - GEIMM
IGF018/94 (human, Caucasian, Krabbe disease) - GEIMM
IGF018/95 (human, Caucasian) - GEIMM
IGF018/96 (human, Caucasian) - GEIMM
IGF018/97 (human, Caucasian) - GEIMM
IGF018/98 (human, Caucasian) - GEIMM
IGF018/99 (human, Caucasian) - GEIMM
IGF019/00 (human, Caucasian) - GEIMM
IGF019/01 (human, Caucasian) - GEIMM
IGF019/77 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF019/78 (human, Caucasian) - GEIMM
IGF019/80 (human, Caucasian, neuroaxonal dystrophy, infantile) - GEIMM
IGF019/82 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF019/84 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF019/85 (human, Caucasian) - GEIMM
IGF019/86 (human, Caucasian) - GEIMM
IGF019/87 (human, Caucasian, ataxia telangiectasia) - GEIMM
IGF019/88 (human, Caucasian) - GEIMM
IGF019/89 (human, Caucasian) - GEIMM
IGF019/90 (human, Caucasian, osteogenesis imperfecta) - GEIMM
IGF019/91 (human, Caucasian) - GEIMM
IGF019/92 (human, Caucasian) - GEIMM
IGF019/93 (human, Caucasian, homocystinuria - megaloblastic anemia) - GEIMM
IGF019/96 (human, Caucasian, acyl-CoA dehydrogenase, long-chain, deficiency) - GEIMM
IGF019/97 (human, Caucasian) - GEIMM
IGF019/98 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF019/99 (human, Caucasian) - GEIMM
IGF020/00 (human, Caucasian, SURF1) - GEIMM
IGF020/01 (human, Caucasian) - GEIMM
IGF020/78 (human, Caucasian) - GEIMM
IGF020/80 (human, Caucasian) - GEIMM
IGF020/82 (human, Caucasian) - GEIMM
IGF020/83 (human, Caucasian, multiple carboxylase deficiency, late-onset) - GEIMM
IGF020/84 (human, Caucasian, Krabbe disease) - GEIMM
IGF020/85 (human, Caucasian) - GEIMM
IGF020/86 (human, Caucasian) - GEIMM
IGF020/87 (human, Caucasian) - GEIMM
IGF020/88 (human, Caucasian) - GEIMM
IGF020/89 (human, Caucasian) - GEIMM
IGF020/90 (human, Caucasian) - GEIMM
IGF020/91 (human, Caucasian) - GEIMM
IGF020/92 (human, Caucasian) - GEIMM
IGF020/93 (human, Caucasian, Krabbe disease) - GEIMM
IGF020/94 (human, Caucasian, homocystinuria - megaloblastic anemia) - GEIMM
IGF020/95 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF020/96 (human, Caucasian, proteolipid protein, myelin) - GEIMM
IGF020/97 (human, Caucasian, mucolipidosis II) - GEIMM
IGF020/98 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF020/99 (human, Caucasian) - GEIMM
IGF021/00 (human, Caucasian) - GEIMM
IGF021/01 (human, Caucasian) - GEIMM
IGF021/78 (human, Caucasian) - GEIMM
IGF021/82 (human, Caucasian) - GEIMM
IGF021/83 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF021/84 (human, Caucasian, mucolipidosis II) - GEIMM
IGF021/85 (human, Caucasian) - GEIMM
IGF021/86 (human, Caucasian, Kartagener syndrome X) - GEIMM
IGF021/87 (human, Caucasian, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF021/88 (human, Caucasian) - GEIMM
IGF021/90 (human, Caucasian) - GEIMM
IGF021/91 (human, Caucasian) - GEIMM
IGF021/92 (human, Caucasian) - GEIMM
IGF021/93 (human, Caucasian) - GEIMM
IGF021/94 (human, Caucasian, fructose-1, 6-diphosphatase deficiency) - GEIMM
IGF021/95 (human, Caucasian) - GEIMM
IGF021/96 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF021/97 (human, Caucasian) - GEIMM
IGF021/98 (human, Caucasian) - GEIMM
IGF021/99 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF022/00 (human, Caucasian) - GEIMM
IGF022/01 (human, Caucasian) - GEIMM
IGF022/77 (human, Caucasian) - GEIMM
IGF022/78 (human, Caucasian) - GEIMM
IGF022/79 (human, Caucasian) - GEIMM
IGF022/80 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF022/81 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF022/82 (human, Caucasian) - GEIMM
IGF022/83 (human, Caucasian) - GEIMM
IGF022/84 (human, Caucasian) - GEIMM
IGF022/85 (human, Caucasian) - GEIMM
IGF022/86 (human, Caucasian, Sandhoff disease) - GEIMM
IGF022/87 (human, Caucasian, Lesch-Nyhan syndrome) - GEIMM
IGF022/88 (human, Caucasian) - GEIMM
IGF022/89 (human, Caucasian, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF022/90 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF022/91 (human, Caucasian) - GEIMM
IGF022/92 (human, Caucasian) - GEIMM
IGF022/93 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF022/94 (human, Caucasian, methylmalonicacidemia) - GEIMM
IGF022/95 (human, Caucasian) - GEIMM
IGF022/96 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF022/97 (human, Caucasian) - GEIMM
IGF022/98 (human, Caucasian) - GEIMM
IGF022/99 (human, Caucasian) - GEIMM
IGF023/00 (human, Caucasian) - GEIMM
IGF023/01 (human, Caucasian) - GEIMM
IGF023/77 (human, Caucasian) - GEIMM
IGF023/78 (human, Caucasian) - GEIMM
IGF023/79 (human, Caucasian) - GEIMM
IGF023/81 (human, Caucasian) - GEIMM
IGF023/83 (human, Caucasian, Fanconi-Bickel syndrome) - GEIMM
IGF023/84 (human, Caucasian, Engelmann disease) - GEIMM
IGF023/85 (human, Caucasian, glycogen storage disease III) - GEIMM
IGF023/86 (human, Caucasian, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF023/87 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF023/88 (human, Caucasian, mucolipidosis II) - GEIMM
IGF023/90 (human, Caucasian) - GEIMM
IGF023/91 (human, Caucasian) - GEIMM
IGF023/93 (human, Caucasian) - GEIMM
IGF023/94 (human, Caucasian) - GEIMM
IGF023/95 (human, Caucasian) - GEIMM
IGF023/96 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF023/97 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF023/98 (human, Caucasian) - GEIMM
IGF023/99 (human, Caucasian) - GEIMM
IGF024/00 (human, Caucasian, citrullinemia) - GEIMM
IGF024/01 (human, Caucasian) - GEIMM
IGF024/77 (human, Caucasian, neuraminidase deficiency) - GEIMM
IGF024/78 (human, Caucasian) - GEIMM
IGF024/79 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF024/81 (human, Caucasian, dibasicaminoaciduria II) - GEIMM
IGF024/82 (human, Caucasian) - GEIMM
IGF024/83 (human, Caucasian) - GEIMM
IGF024/85 (human, Caucasian, glycogen storage disease III) - GEIMM
IGF024/86 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF024/88 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF024/90 (human, Caucasian) - GEIMM
IGF024/91 (human, Caucasian) - GEIMM
IGF024/92 (human, Caucasian) - GEIMM
IGF024/93 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF024/94 (human, Caucasian) - GEIMM
IGF024/95 (human, Caucasian) - GEIMM
IGF024/96 (human, Caucasian) - GEIMM
IGF024/97 (human, Caucasian) - GEIMM
IGF024/98 (human, Caucasian) - GEIMM
IGF024/99 (human, Caucasian) - GEIMM
IGF025/00 (human, Caucasian) - GEIMM
IGF025/01 (human, Caucasian) - GEIMM
IGF025/77 (human, Caucasian, neuraminidase deficiency) - GEIMM
IGF025/78 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF025/80 (human, Caucasian) - GEIMM
IGF025/81 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF025/82 (human, Caucasian, mucopolysaccharidosis type III C) - GEIMM
IGF025/83 (human, Caucasian) - GEIMM
IGF025/84 (human, Caucasian) - GEIMM
IGF025/85 (human, Caucasian, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF025/86 (human, Caucasian) - GEIMM
IGF025/87 (human, Caucasian) - GEIMM
IGF025/88 (human, Caucasian, mucopolysaccharidosis type VI) - GEIMM
IGF025/89 (human, Caucasian, Krabbe disease) - GEIMM
IGF025/90 (human, Caucasian) - GEIMM
IGF025/91 (human, Caucasian, acyl-CoA dehydrogenase, long-chain, deficiency) - GEIMM
IGF025/92 (human, Caucasian, arthrogryposis multiplex congenita) - GEIMM
IGF025/93 (human, Caucasian) - GEIMM
IGF025/95 (human, Caucasian, fucosidosis) - GEIMM
IGF025/96 (human, Caucasian, mucolipidosis II) - GEIMM
IGF025/97 (human, Caucasian) - GEIMM
IGF025/98 (human, Caucasian, cystic fibrosis) - GEIMM
IGF025/99 (human, Caucasian, Gaucher disease type II) - GEIMM
IGF026/00 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF026/01 (human, Caucasian) - GEIMM
IGF026/77 (human, Caucasian) - GEIMM
IGF026/78 (human, Caucasian, mucolipidosis II) - GEIMM
IGF026/80 (human, Caucasian) - GEIMM
IGF026/82 (human, Caucasian) - GEIMM
IGF026/83 (human, Caucasian) - GEIMM
IGF026/84 (human, Caucasian) - GEIMM
IGF026/85 (human, Caucasian) - GEIMM
IGF026/86 (human, Caucasian, Gaucher disease type III) - GEIMM
IGF026/87 (human, Caucasian) - GEIMM
IGF026/88 (human, Caucasian, neuraminidase deficiency) - GEIMM
IGF026/89 (human, Caucasian) - GEIMM
IGF026/90 (human, Caucasian, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF026/91 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF026/92 (human, Caucasian) - GEIMM
IGF026/93 (human, Caucasian) - GEIMM
IGF026/95 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF026/96 (human, Caucasian) - GEIMM
IGF026/97 (human, Caucasian) - GEIMM
IGF026/98 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF026/99 (human, Caucasian, Gaucher disease type II) - GEIMM
IGF027/00 (human, Caucasian, mucolipidosis II) - GEIMM
IGF027/01 (human, Caucasian) - GEIMM
IGF027/77 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF027/78 (human, Caucasian) - GEIMM
IGF027/80 (human, Caucasian) - GEIMM
IGF027/82 (human, Caucasian) - GEIMM
IGF027/83 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF027/84 (human, Caucasian) - GEIMM
IGF027/85 (human, Caucasian) - GEIMM
IGF027/86 (human, Caucasian) - GEIMM
IGF027/87 (human, Caucasian) - GEIMM
IGF027/88 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF027/89 (human, Caucasian) - GEIMM
IGF027/90 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF027/91 (human, Caucasian) - GEIMM
IGF027/92 (human, Caucasian) - GEIMM
IGF027/93 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF027/94 (human, Caucasian) - GEIMM
IGF027/95 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF027/96 (human, Caucasian) - GEIMM
IGF027/97 (human, Caucasian) - GEIMM
IGF027/98 (human, Caucasian) - GEIMM
IGF027/99 (human, Caucasian) - GEIMM
IGF028/00 (human, Caucasian, spongy degeneration of central nervous system /Canavan disease) - GEIMM
IGF028/01 (human, Caucasian) - GEIMM
IGF028/77 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF028/78 (human, Caucasian) - GEIMM
IGF028/80 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF028/81 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF028/82 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF028/83 (human, Caucasian) - GEIMM
IGF028/84 (human, Caucasian) - GEIMM
IGF028/85 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF028/86 (human, Caucasian) - GEIMM
IGF028/87 (human, Caucasian) - GEIMM
IGF028/88 (human, Caucasian) - GEIMM
IGF028/89 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF028/91 (human, Caucasian) - GEIMM
IGF028/92 (human, Caucasian, sialic acid storage disease) - GEIMM
IGF028/93 (human, Caucasian) - GEIMM
IGF028/95 (human, Caucasian, methylmalonicacidemia) - GEIMM
IGF028/97 (human, Caucasian) - GEIMM
IGF028/98 (human, Caucasian, Krabbe disease) - GEIMM
IGF028/99 (human, Caucasian) - GEIMM
IGF029/00 (human, Caucasian) - GEIMM
IGF029/01 (human, Caucasian) - GEIMM
IGF029/77 (human, Caucasian, arsa pseudodeficiency) - GEIMM
IGF029/78 (human, Caucasian) - GEIMM
IGF029/81 (human, Caucasian, homocystinuria) - GEIMM
IGF029/82 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF029/83 (human, Caucasian, arsa pseudodeficiency) - GEIMM
IGF029/85 (human, Caucasian, gangliosidosis, generalized GM1, type II) - GEIMM
IGF029/86 (human, Caucasian) - GEIMM
IGF029/87 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF029/88 (human, Caucasian) - GEIMM
IGF029/89 (human, Caucasian) - GEIMM
IGF029/91 (human, Caucasian) - GEIMM
IGF029/92 (human, Caucasian, spastic paraparesis) - GEIMM
IGF029/93 (human, Caucasian, methylmalonicacidemia) - GEIMM
IGF029/97 (human, Caucasian) - GEIMM
IGF029/98 (human, Caucasian, mucolipidosis II) - GEIMM
IGF029/99 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF030/00 (human, Caucasian) - GEIMM
IGF030/01 (human, Caucasian) - GEIMM
IGF030/77 (human, Caucasian) - GEIMM
IGF030/78 (human, Caucasian) - GEIMM
IGF030/80 (human, Caucasian) - GEIMM
IGF030/83 (human, Caucasian) - GEIMM
IGF030/84 (human, Caucasian) - GEIMM
IGF030/85 (human, Caucasian) - GEIMM
IGF030/86 (human, Caucasian) - GEIMM
IGF030/87 (human, Caucasian) - GEIMM
IGF030/88 (human, Caucasian) - GEIMM
IGF030/89 (human, Caucasian) - GEIMM
IGF030/91 (human, Caucasian) - GEIMM
IGF030/92 (human, Caucasian) - GEIMM
IGF030/94 (human, Caucasian) - GEIMM
IGF030/96 (human, Caucasian) - GEIMM
IGF030/97 (human, Caucasian) - GEIMM
IGF030/98 (human, Caucasian) - GEIMM
IGF030/99 (human, Caucasian) - GEIMM
IGF031/00 (human, Caucasian, SURF1) - GEIMM
IGF031/01 (human, Caucasian) - GEIMM
IGF031/77 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF031/80 (human, Caucasian, mucopolysaccharidosis type III D) - GEIMM
IGF031/81 (human, Caucasian) - GEIMM
IGF031/83 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF031/84 (human, Caucasian) - GEIMM
IGF031/85 (human, Caucasian, alkaptonuria) - GEIMM
IGF031/86 (human, Caucasian) - GEIMM
IGF031/88 (human, Caucasian) - GEIMM
IGF031/89 (human, Caucasian) - GEIMM
IGF031/90 (human, Caucasian, osteogenesis imperfecta, type I neurofibr.) - GEIMM
IGF031/91 (human, Caucasian) - GEIMM
IGF031/92 (human, Caucasian) - GEIMM
IGF031/93 (human, Caucasian) - GEIMM
IGF031/94 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF031/96 (human, Caucasian, Gaucher disease type II) - GEIMM
IGF031/97 (human, Caucasian, Menkes syndrome) - GEIMM
IGF031/98 (human, Caucasian) - GEIMM
IGF031/99 (human, Caucasian) - GEIMM
IGF032/00 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF032/01 (human, Caucasian) - GEIMM
IGF032/76 (human, Caucasian, neuraminidase deficiency with beta-galactosidase deficiency) - GEIMM
IGF032/77 (human, Caucasian) - GEIMM
IGF032/78 (human, Caucasian) - GEIMM
IGF032/80 (human, Caucasian) - GEIMM
IGF032/81 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF032/82 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF032/83 (human, Caucasian, maple syrup urine disease) - GEIMM
IGF032/84 (human, Caucasian) - GEIMM
IGF032/85 (human, Caucasian, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF032/86 (human, Caucasian) - GEIMM
IGF032/87 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF032/88 (human, Caucasian) - GEIMM
IGF032/89 (human, Caucasian) - GEIMM
IGF032/90 (human, Caucasian) - GEIMM
IGF032/91 (human, Caucasian) - GEIMM
IGF032/93 (human, Caucasian) - GEIMM
IGF032/94 (human, Caucasian, osteogenesis imperfecta) - GEIMM
IGF032/96 (human, Caucasian) - GEIMM
IGF032/97 (human, Caucasian) - GEIMM
IGF032/98 (human, Caucasian) - GEIMM
IGF032/99 (human, Caucasian) - GEIMM
IGF033/00 (human, Caucasian) - GEIMM
IGF033/01 (human, Caucasian) - GEIMM
IGF033/77 (human, Caucasian) - GEIMM
IGF033/78 (human, Caucasian, Sandhoff disease) - GEIMM
IGF033/80 (human, Caucasian) - GEIMM
IGF033/81 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF033/83 (human, Caucasian, fucosidosis) - GEIMM
IGF033/84 (human, Caucasian) - GEIMM
IGF033/85 (human, Caucasian) - GEIMM
IGF033/86 (human, Caucasian, multiple carboxylase deficiency, biotin-responsive) - GEIMM
IGF033/87 (human, Caucasian) - GEIMM
IGF033/88 (human, Caucasian) - GEIMM
IGF033/89 (human, Caucasian, sensorineural deafness) - GEIMM
IGF033/90 (human, Caucasian, COFS syndrome / cerebrooculofacioskeletal syndrome) - GEIMM
IGF033/91 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF033/93 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF033/94 (human, Caucasian) - GEIMM
IGF033/95 (human, Caucasian) - GEIMM
IGF033/96 (human, Caucasian) - GEIMM
IGF033/97 (human, Caucasian, propionicacidemia I) - GEIMM
IGF033/98 (human, Caucasian) - GEIMM
IGF033/99 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF034/00 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF034/01 (human, Caucasian) - GEIMM
IGF034/76 (human, Caucasian, SCID (severe combined immunodeficiency 1)) - GEIMM
IGF034/77 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF034/80 (human, Caucasian) - GEIMM
IGF034/81 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF034/83 (human, Caucasian) - GEIMM
IGF034/84 (human, Caucasian) - GEIMM
IGF034/85 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF034/86 (human, Caucasian) - GEIMM
IGF034/87 (human, Caucasian) - GEIMM
IGF034/88 (human, Caucasian) - GEIMM
IGF034/89 (human, Caucasian) - GEIMM
IGF034/90 (human, Caucasian) - GEIMM
IGF034/91 (human, Caucasian, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF034/92 (human, Caucasian) - GEIMM
IGF034/93 (human, Caucasian) - GEIMM
IGF034/94 (human, Caucasian) - GEIMM
IGF034/95 (human, Caucasian) - GEIMM
IGF034/96 (human, Caucasian) - GEIMM
IGF034/97 (human, Caucasian, argininosuccinicaciduria) - GEIMM
IGF034/98 (human, Caucasian) - GEIMM
IGF034/99 (human, Caucasian) - GEIMM
IGF035/00 (human, Caucasian) - GEIMM
IGF035/01 (human, Caucasian) - GEIMM
IGF035/77 (human, Caucasian, Niemann-Pick disease, type B) - GEIMM
IGF035/80 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF035/81 (human, Caucasian, fucosidosis) - GEIMM
IGF035/82 (human, Caucasian) - GEIMM
IGF035/83 (human, Caucasian) - GEIMM
IGF035/85 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF035/86 (human, Caucasian) - GEIMM
IGF035/87 (human, Caucasian, gangliosidosis, generalized GM1, type II) - GEIMM
IGF035/88 (human, Caucasian, fucosidosis) - GEIMM
IGF035/89 (human, Caucasian) - GEIMM
IGF035/90 (human, Caucasian) - GEIMM
IGF035/91 (human, Caucasian) - GEIMM
IGF035/92 (human, Caucasian, Menkes syndrome) - GEIMM
IGF035/93 (human, Caucasian) - GEIMM
IGF035/94 (human, Caucasian, mucolipidosis III) - GEIMM
IGF035/96 (human, Caucasian) - GEIMM
IGF035/97 (human, Caucasian) - GEIMM
IGF035/98 (human, Caucasian) - GEIMM
IGF035/99 (human, Caucasian) - GEIMM
IGF036/00 (human, Caucasian, Krabbe disease) - GEIMM
IGF036/01 (human, Caucasian) - GEIMM
IGF036/76 (human, Caucasian) - GEIMM
IGF036/77 (human, Caucasian) - GEIMM
IGF036/78 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF036/79 (human, Caucasian, cystic fibrosis) - GEIMM
IGF036/80 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF036/81 (human, Caucasian) - GEIMM
IGF036/83 (human, Caucasian, Krabbe disease) - GEIMM
IGF036/84 (human, Caucasian) - GEIMM
IGF036/86 (human, Caucasian) - GEIMM
IGF036/87 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF036/88 (human, Caucasian, osteogenesis imperfecta, type II) - GEIMM
IGF036/89 (human, Caucasian) - GEIMM
IGF036/90 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF036/92 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF036/93 (human, Caucasian) - GEIMM
IGF036/94 (human, Caucasian) - GEIMM
IGF036/96 (human, Caucasian) - GEIMM
IGF036/97 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF036/98 (human, Caucasian) - GEIMM
IGF036/99 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF037/00 (human, Caucasian) - GEIMM
IGF037/01 (human, Caucasian) - GEIMM
IGF037/76 (human, Caucasian) - GEIMM
IGF037/77 (human, Caucasian) - GEIMM
IGF037/78 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF037/80 (human, Caucasian) - GEIMM
IGF037/82 (human, Caucasian) - GEIMM
IGF037/83 (human, Caucasian) - GEIMM
IGF037/84 (human, Caucasian, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF037/85 (human, Caucasian) - GEIMM
IGF037/86 (human, Caucasian, myopathy with deficiency of CPT I) - GEIMM
IGF037/87 (human, Caucasian) - GEIMM
IGF037/91 (human, Caucasian) - GEIMM
IGF037/92 (human, Caucasian) - GEIMM
IGF037/93 (human, Caucasian) - GEIMM
IGF037/94 (human, Caucasian, aspartylglycosaminuria) - GEIMM
IGF037/95 (human, Caucasian, molybdenum cofactor deficiency) - GEIMM
IGF037/97 (human, Caucasian, Sandhoff disease) - GEIMM
IGF037/98 (human, African, mucopolysaccharidosis type II) - GEIMM
IGF037/99 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF038/00 (human, Caucasian) - GEIMM
IGF038/01 (human, Caucasian) - GEIMM
IGF038/80 (human, Caucasian, Niemann-Pick disease, type B) - GEIMM
IGF038/81 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF038/82 (human, Caucasian) - GEIMM
IGF038/83 (human, Caucasian) - GEIMM
IGF038/84 (human, Caucasian) - GEIMM
IGF038/85 (human, Caucasian) - GEIMM
IGF038/86 (human, Caucasian, Roberts syndrome) - GEIMM
IGF038/87 (human, Caucasian) - GEIMM
IGF038/88 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF038/89 (human, Caucasian, isovalericacidemia) - GEIMM
IGF038/90 (human, Caucasian) - GEIMM
IGF038/91 (human, Caucasian, Charcot-Marie-Tooth disease) - GEIMM
IGF038/92 (human, Caucasian) - GEIMM
IGF038/93 (human, Caucasian, Turner syndrome, mosaic) - GEIMM
IGF038/95 (human, Caucasian, encephalomyopaty mitocondrial) - GEIMM
IGF038/96 (human, Caucasian, Gaucher disease type II) - GEIMM
IGF038/97 (human, Caucasian) - GEIMM
IGF038/98 (human, Caucasian) - GEIMM
IGF038/99 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF039/00 (human, Caucasian) - GEIMM
IGF039/01 (human, Caucasian) - GEIMM
IGF039/77 (human, Caucasian) - GEIMM
IGF039/80 (human, Caucasian) - GEIMM
IGF039/81 (human, Caucasian, mucolipidosis II) - GEIMM
IGF039/82 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF039/83 (human, Caucasian) - GEIMM
IGF039/84 (human, Caucasian) - GEIMM
IGF039/85 (human, Caucasian, Ehlers-Danlos syndrome) - GEIMM
IGF039/86 (human, Caucasian) - GEIMM
IGF039/87 (human, Caucasian) - GEIMM
IGF039/88 (human, Caucasian) - GEIMM
IGF039/90 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF039/91 (human, Caucasian, Angelman syndrome) - GEIMM
IGF039/92 (human, Caucasian) - GEIMM
IGF039/93 (human, Caucasian, histiocytosis X) - GEIMM
IGF039/94 (human, Caucasian) - GEIMM
IGF039/95 (human, Caucasian) - GEIMM
IGF039/96 (human, Caucasian) - GEIMM
IGF039/97 (human, Caucasian) - GEIMM
IGF039/98 (human, Caucasian) - GEIMM
IGF039/99 (human, Caucasian, mucopolysaccharidosis type III C) - GEIMM
IGF040/00 (human, Caucasian) - GEIMM
IGF040/01 (human, Caucasian) - GEIMM
IGF040/77 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF040/78 (human, Caucasian) - GEIMM
IGF040/79 (human, Caucasian) - GEIMM
IGF040/80 (human, Caucasian) - GEIMM
IGF040/82 (human, Caucasian) - GEIMM
IGF040/83 (human, Caucasian) - GEIMM
IGF040/84 (human, Caucasian) - GEIMM
IGF040/85 (human, Caucasian, Niemann-Pick disease, type B) - GEIMM
IGF040/86 (human, Caucasian) - GEIMM
IGF040/87 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF040/89 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF040/90 (human, Caucasian, Krabbe disease) - GEIMM
IGF040/91 (human, Caucasian) - GEIMM
IGF040/92 (human, Caucasian) - GEIMM
IGF040/93 (human, Caucasian) - GEIMM
IGF040/94 (human, Caucasian) - GEIMM
IGF040/95 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF040/96 (human, Caucasian, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF040/97 (human, Caucasian, mannosidosis, alpha b, lysosomal) - GEIMM
IGF040/98 (human, Caucasian) - GEIMM
IGF040/99 (human, Caucasian) - GEIMM
IGF041/00 (human, Caucasian) - GEIMM
IGF041/01 (human, Caucasian) - GEIMM
IGF041/77 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF041/78 (human, Caucasian) - GEIMM
IGF041/80 (human, Caucasian, ichthyosis X-linked) - GEIMM
IGF041/81 (human, Caucasian) - GEIMM
IGF041/84 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF041/85 (human, Caucasian) - GEIMM
IGF041/86 (human, Caucasian, hyperglycerolemia) - GEIMM
IGF041/87 (human, Caucasian, mucolipidosis II) - GEIMM
IGF041/88 (human, Caucasian) - GEIMM
IGF041/89 (human, Caucasian) - GEIMM
IGF041/90 (human, Caucasian, geleophysic dwarfism) - GEIMM
IGF041/91 (human, Caucasian) - GEIMM
IGF041/92 (human, Caucasian) - GEIMM
IGF041/94 (human, Caucasian, maple syrup urine disease) - GEIMM
IGF041/95 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF041/96 (human, Caucasian) - GEIMM
IGF041/97 (human, Caucasian) - GEIMM
IGF041/98 (human, Caucasian) - GEIMM
IGF041/99 (human, Caucasian) - GEIMM
IGF042/00 (human, Caucasian) - GEIMM
IGF042/01 (human, Caucasian) - GEIMM
IGF042/77 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF042/80 (human, Caucasian) - GEIMM
IGF042/81 (human, Caucasian) - GEIMM
IGF042/82 (human, Caucasian) - GEIMM
IGF042/83 (human, Caucasian) - GEIMM
IGF042/84 (human, Caucasian) - GEIMM
IGF042/85 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF042/86 (human, Caucasian) - GEIMM
IGF042/87 (human, Caucasian) - GEIMM
IGF042/88 (human, Caucasian) - GEIMM
IGF042/89 (human, Caucasian, mucolipidosis II) - GEIMM
IGF042/90 (human, Caucasian, encephalopathy) - GEIMM
IGF042/91 (human, Caucasian) - GEIMM
IGF042/92 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF042/93 (human, Caucasian, Gaucher disease type II) - GEIMM
IGF042/94 (human, Caucasian, Krabbe disease) - GEIMM
IGF042/95 (human, Caucasian) - GEIMM
IGF042/96 (human, Caucasian) - GEIMM
IGF042/97 (human, Caucasian) - GEIMM
IGF042/98 (human, Caucasian) - GEIMM
IGF042/99 (human, Caucasian) - GEIMM
IGF043/00 (human, Caucasian) - GEIMM
IGF043/77 (human, Caucasian) - GEIMM
IGF043/78 (human, Caucasian, ichthyosis X-linked) - GEIMM
IGF043/79 (human, Caucasian) - GEIMM
IGF043/80 (human, Caucasian) - GEIMM
IGF043/81 (human, Caucasian) - GEIMM
IGF043/82 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF043/84 (human, Caucasian) - GEIMM
IGF043/85 (human, Caucasian) - GEIMM
IGF043/86 (human, Caucasian) - GEIMM
IGF043/88 (human, Caucasian) - GEIMM
IGF043/89 (human, Caucasian) - GEIMM
IGF043/90 (human, Caucasian) - GEIMM
IGF043/91 (human, Caucasian, arsa pseudodeficiency) - GEIMM
IGF043/92 (human, Caucasian) - GEIMM
IGF043/93 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF043/94 (human, Caucasian) - GEIMM
IGF043/96 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF043/97 (human, Caucasian) - GEIMM
IGF043/98 (human, Caucasian) - GEIMM
IGF043/99 (human, Caucasian) - GEIMM
IGF044/00 (human, Caucasian) - GEIMM
IGF044/77 (human, Caucasian) - GEIMM
IGF044/78 (human, Caucasian) - GEIMM
IGF044/79 (human, Caucasian) - GEIMM
IGF044/81 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF044/82 (human, Caucasian) - GEIMM
IGF044/83 (human, Caucasian, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF044/84 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF044/85 (human, Caucasian) - GEIMM
IGF044/86 (human, Caucasian, Marfan syndrome) - GEIMM
IGF044/87 (human, Caucasian) - GEIMM
IGF044/88 (human, Caucasian) - GEIMM
IGF044/89 (human, Caucasian) - GEIMM
IGF044/90 (human, Caucasian) - GEIMM
IGF044/91 (human, Caucasian) - GEIMM
IGF044/92 (human, Caucasian) - GEIMM
IGF044/93 (human, Caucasian) - GEIMM
IGF044/94 (human, Caucasian) - GEIMM
IGF044/95 (human, Caucasian, Gaucher disease type II) - GEIMM
IGF044/96 (human, Caucasian) - GEIMM
IGF044/97 (human, Caucasian) - GEIMM
IGF044/98 (human, Caucasian) - GEIMM
IGF044/99 (human, Caucasian) - GEIMM
IGF045/00 (human, Caucasian) - GEIMM
IGF045/78 (human, Caucasian) - GEIMM
IGF045/79 (human, Caucasian, mucolipidosis III) - GEIMM
IGF045/80 (human, Caucasian) - GEIMM
IGF045/81 (human, Caucasian) - GEIMM
IGF045/82 (human, Caucasian) - GEIMM
IGF045/83 (human, Caucasian) - GEIMM
IGF045/84 (human, Caucasian) - GEIMM
IGF045/85 (human, Caucasian) - GEIMM
IGF045/86 (human, Caucasian) - GEIMM
IGF045/87 (human, Caucasian) - GEIMM
IGF045/88 (human, Caucasian) - GEIMM
IGF045/89 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF045/90 (human, Caucasian, osteogenesis imperfecta, type II) - GEIMM
IGF045/91 (human, Caucasian) - GEIMM
IGF045/92 (human, Caucasian) - GEIMM
IGF045/93 (human, Caucasian) - GEIMM
IGF045/94 (human, Caucasian) - GEIMM
IGF045/95 (human, Caucasian) - GEIMM
IGF045/96 (human, Caucasian) - GEIMM
IGF045/97 (human, Caucasian) - GEIMM
IGF045/98 (human, Caucasian) - GEIMM
IGF045/99 (human, Caucasian) - GEIMM
IGF046/00 (human, Caucasian) - GEIMM
IGF046/76 (human, Caucasian) - GEIMM
IGF046/78 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF046/79 (human, Caucasian) - GEIMM
IGF046/80 (human, Caucasian) - GEIMM
IGF046/81 (human, South American) - GEIMM
IGF046/82 (human, Caucasian, Coffin-Lowry syndrome) - GEIMM
IGF046/83 (human, Caucasian) - GEIMM
IGF046/84 (human, Caucasian) - GEIMM
IGF046/85 (human, Caucasian) - GEIMM
IGF046/87 (human, Caucasian) - GEIMM
IGF046/89 (human, Caucasian, osteogenesis imperfecta, type II) - GEIMM
IGF046/90 (human, Caucasian, Krabbe disease) - GEIMM
IGF046/91 (human, Caucasian) - GEIMM
IGF046/92 (human, Caucasian, dystrophy congenital progressive) - GEIMM
IGF046/93 (human, Caucasian) - GEIMM
IGF046/94 (human, Caucasian) - GEIMM
IGF046/95 (human, Caucasian, Costello syndrome) - GEIMM
IGF046/96 (human, Caucasian) - GEIMM
IGF046/97 (human, Caucasian) - GEIMM
IGF046/98 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF046/99 (human, Caucasian) - GEIMM
IGF047/00 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF047/78 (human, Caucasian, Gaucher disease type III) - GEIMM
IGF047/80 (human, Caucasian) - GEIMM
IGF047/82 (human, Caucasian, phenylketonuria II) - GEIMM
IGF047/83 (human, Caucasian) - GEIMM
IGF047/84 (human, Caucasian) - GEIMM
IGF047/85 (human, Caucasian) - GEIMM
IGF047/86 (human, Caucasian) - GEIMM
IGF047/87 (human, Caucasian) - GEIMM
IGF047/88 (human, Caucasian) - GEIMM
IGF047/89 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF047/90 (human, Caucasian) - GEIMM
IGF047/91 (human, Caucasian) - GEIMM
IGF047/92 (human, Caucasian, osteogenesis imperfecta, type II) - GEIMM
IGF047/94 (human, Caucasian) - GEIMM
IGF047/95 (human, Caucasian, mucopolysaccharidosis type VI) - GEIMM
IGF047/96 (human, Caucasian, maple syrup urine disease) - GEIMM
IGF047/97 (human, Caucasian) - GEIMM
IGF047/98 (human, Caucasian, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF047/99 (human, Caucasian) - GEIMM
IGF048/77 (human, Caucasian) - GEIMM
IGF048/79 (human, Caucasian) - GEIMM
IGF048/80 (human, Caucasian, aspartylglycosaminuria) - GEIMM
IGF048/82 (human, Caucasian, galactosemia) - GEIMM
IGF048/83 (human, Caucasian) - GEIMM
IGF048/84 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF048/85 (human, Caucasian) - GEIMM
IGF048/86 (human, Caucasian, Niemann-Pick disease, type B) - GEIMM
IGF048/89 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF048/90 (human, Caucasian) - GEIMM
IGF048/91 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF048/94 (human, Caucasian, Marfan syndrome) - GEIMM
IGF048/95 (human, Caucasian) - GEIMM
IGF048/96 (human, Caucasian, muscolar dystrophy def.sarcoglican) - GEIMM
IGF048/97 (human, Caucasian) - GEIMM
IGF048/98 (human, Caucasian) - GEIMM
IGF048/99 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF049/00 (human, Caucasian) - GEIMM
IGF049/77 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF049/78 (human, Caucasian) - GEIMM
IGF049/79 (human, Caucasian, Gaucher disease type III) - GEIMM
IGF049/80 (human, Caucasian) - GEIMM
IGF049/82 (human, Caucasian) - GEIMM
IGF049/83 (human, Caucasian) - GEIMM
IGF049/84 (human, Caucasian) - GEIMM
IGF049/85 (human, Caucasian) - GEIMM
IGF049/86 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF049/87 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF049/89 (human, Caucasian, homocystinuria) - GEIMM
IGF049/90 (human, Caucasian, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF049/91 (human, Caucasian, hypercholesterolemia, familial) - GEIMM
IGF049/92 (human, Caucasian) - GEIMM
IGF049/93 (human, Caucasian, Krabbe disease) - GEIMM
IGF049/94 (human, Caucasian) - GEIMM
IGF049/95 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF049/96 (human, Caucasian, SCID (severe combined immunodeficiency 1)) - GEIMM
IGF049/97 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF049/98 (human, Caucasian) - GEIMM
IGF049/99 (human, Caucasian, methylenetetra-hydrofolate reductase def.) - GEIMM
IGF050/00 (human, Caucasian, Costello syndrome) - GEIMM
IGF050/76 (human, Caucasian, fructose intolerance, hereditary) - GEIMM
IGF050/77 (human, Caucasian) - GEIMM
IGF050/78 (human, Caucasian) - GEIMM
IGF050/80 (human, Caucasian) - GEIMM
IGF050/83 (human, Caucasian) - GEIMM
IGF050/84 (human, Caucasian) - GEIMM
IGF050/85 (human, Caucasian) - GEIMM
IGF050/86 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF050/87 (human, Caucasian) - GEIMM
IGF050/90 (human, Caucasian, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF050/91 (human, Caucasian) - GEIMM
IGF050/92 (human, Caucasian, Aicardi syndrome / corpus callosum) - GEIMM
IGF050/93 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF050/97 (human, Caucasian) - GEIMM
IGF050/98 (human, Caucasian) - GEIMM
IGF050/99 (human, Caucasian) - GEIMM
IGF051/00 (human, Caucasian) - GEIMM
IGF051/77 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF051/78 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF051/80 (human, Caucasian) - GEIMM
IGF051/82 (human, Caucasian, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF051/83 (human, Caucasian) - GEIMM
IGF051/84 (human, Caucasian) - GEIMM
IGF051/85 (human, Caucasian, osteogenesis imperfecta, type I (with blue sclerae)) - GEIMM
IGF051/86 (human, Caucasian) - GEIMM
IGF051/87 (human, Caucasian) - GEIMM
IGF051/88 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF051/89 (human, Caucasian) - GEIMM
IGF051/90 (human, Caucasian) - GEIMM
IGF051/91 (human, Caucasian, dibasicaminoaciduria II) - GEIMM
IGF051/92 (human, Caucasian, mucopolysaccharidosis type VI) - GEIMM
IGF051/93 (human, Caucasian, mucolipidosis II) - GEIMM
IGF051/94 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF051/95 (human, Caucasian) - GEIMM
IGF051/97 (human, Caucasian, pycnodysostosis) - GEIMM
IGF051/98 (human, Caucasian) - GEIMM
IGF051/99 (human, Caucasian) - GEIMM
IGF052/00 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF052/76 (human, Caucasian) - GEIMM
IGF052/77 (human, Caucasian) - GEIMM
IGF052/78 (human, Caucasian) - GEIMM
IGF052/80 (human, Caucasian) - GEIMM
IGF052/81 (human, Caucasian) - GEIMM
IGF052/82 (human, Caucasian) - GEIMM
IGF052/83 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF052/84 (human, Caucasian) - GEIMM
IGF052/85 (human, Caucasian, osteogenesis imperfecta, type I (with blue sclerae)) - GEIMM
IGF052/86 (human, Caucasian, ataxia telangiectasia) - GEIMM
IGF052/87 (human, Caucasian) - GEIMM
IGF052/88 (human, Caucasian) - GEIMM
IGF052/89 (human, Caucasian, hemochromatosis neonatal) - GEIMM
IGF052/90 (human, Caucasian) - GEIMM
IGF052/91 (human, Caucasian) - GEIMM
IGF052/92 (human, Caucasian) - GEIMM
IGF052/93 (human, Caucasian, Costello syndrome) - GEIMM
IGF052/94 (human, Caucasian) - GEIMM
IGF052/95 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF052/97 (human, Caucasian) - GEIMM
IGF052/99 (human, Caucasian) - GEIMM
IGF053/00 (human, Caucasian) - GEIMM
IGF053/78 (human, Caucasian) - GEIMM
IGF053/80 (human, Caucasian) - GEIMM
IGF053/81 (human, Caucasian) - GEIMM
IGF053/83 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF053/84 (human, Caucasian) - GEIMM
IGF053/85 (human, Caucasian) - GEIMM
IGF053/86 (human, Caucasian) - GEIMM
IGF053/87 (human, Caucasian) - GEIMM
IGF053/89 (human, Caucasian) - GEIMM
IGF053/90 (human, Caucasian) - GEIMM
IGF053/91 (human, Caucasian) - GEIMM
IGF053/92 (human, Caucasian) - GEIMM
IGF053/94 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF053/97 (human, Caucasian) - GEIMM
IGF053/99 (human, Caucasian) - GEIMM
IGF054/77 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF054/78 (human, Caucasian) - GEIMM
IGF054/80 (human, Caucasian) - GEIMM
IGF054/82 (human, Caucasian) - GEIMM
IGF054/83 (human, Caucasian) - GEIMM
IGF054/84 (human, Caucasian) - GEIMM
IGF054/85 (human, Caucasian) - GEIMM
IGF054/86 (human, Caucasian) - GEIMM
IGF054/89 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF054/90 (human, Caucasian) - GEIMM
IGF054/91 (human, Caucasian, dibasicaminoaciduria II) - GEIMM
IGF054/92 (human, Caucasian, glycogen storage disease III) - GEIMM
IGF054/93 (human, Caucasian, fucosidosis) - GEIMM
IGF054/94 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF054/95 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF054/97 (human, Caucasian, pycnodysostosis) - GEIMM
IGF054/99 (human, Caucasian) - GEIMM
IGF055/77 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF055/78 (human, Caucasian) - GEIMM
IGF055/80 (human, Caucasian) - GEIMM
IGF055/83 (human, Caucasian) - GEIMM
IGF055/84 (human, Caucasian) - GEIMM
IGF055/86 (human, Caucasian) - GEIMM
IGF055/87 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF055/88 (human, Caucasian, factor XIII deficiency) - GEIMM
IGF055/89 (human, Caucasian, trisomy 21 / Down syndrome) - GEIMM
IGF055/90 (human, Caucasian) - GEIMM
IGF055/92 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF055/93 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF055/94 (human, Caucasian) - GEIMM
IGF055/95 (human, Caucasian) - GEIMM
IGF055/97 (human, Caucasian, neuraminidase deficiency) - GEIMM
IGF055/99 (human, Caucasian) - GEIMM
IGF056/78 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF056/79 (human, Caucasian, cystic fibrosis) - GEIMM
IGF056/80 (human, Caucasian) - GEIMM
IGF056/81 (human, Caucasian, glycogen storage disease III) - GEIMM
IGF056/82 (human, Caucasian) - GEIMM
IGF056/83 (human, Caucasian) - GEIMM
IGF056/85 (human, Caucasian) - GEIMM
IGF056/87 (human, Caucasian, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF056/90 (human, Caucasian) - GEIMM
IGF056/91 (human, Caucasian, chondrodysplasia punctata) - GEIMM
IGF056/92 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF056/93 (human, Caucasian, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF056/94 (human, Caucasian) - GEIMM
IGF056/95 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF056/97 (human, Caucasian) - GEIMM
IGF057/76 (human, Caucasian) - GEIMM
IGF057/77 (human, Caucasian) - GEIMM
IGF057/78 (human, Caucasian) - GEIMM
IGF057/80 (human, Caucasian) - GEIMM
IGF057/81 (human, Caucasian) - GEIMM
IGF057/82 (human, Caucasian) - GEIMM
IGF057/83 (human, Caucasian) - GEIMM
IGF057/84 (human, Caucasian) - GEIMM
IGF057/85 (human, Caucasian) - GEIMM
IGF057/86 (human, Caucasian) - GEIMM
IGF057/87 (human, Caucasian) - GEIMM
IGF057/88 (human, Caucasian) - GEIMM
IGF057/89 (human, Caucasian) - GEIMM
IGF057/90 (human, Caucasian) - GEIMM
IGF057/91 (human, Caucasian, Ehlers-Danlos syndrome, type I) - GEIMM
IGF057/92 (human, Caucasian, Zellweger syndrome) - GEIMM
IGF057/93 (human, Caucasian) - GEIMM
IGF057/95 (human, Caucasian) - GEIMM
IGF057/97 (human, Caucasian, mucolipidosis II) - GEIMM
IGF058/78 (human, Caucasian) - GEIMM
IGF058/79 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF058/80 (human, Caucasian) - GEIMM
IGF058/82 (human, Caucasian) - GEIMM
IGF058/83 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF058/84 (human, Caucasian) - GEIMM
IGF058/85 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF058/86 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF058/87 (human, Caucasian) - GEIMM
IGF058/89 (human, Caucasian) - GEIMM
IGF058/90 (human, Caucasian, osteogenesis imperfecta) - GEIMM
IGF058/91 (human, Caucasian) - GEIMM
IGF058/93 (human, Caucasian) - GEIMM
IGF058/95 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF058/97 (human, Caucasian) - GEIMM
IGF059/76 (human, Caucasian, mucolipidosis II) - GEIMM
IGF059/78 (human, Caucasian) - GEIMM
IGF059/79 (human, Caucasian, gangliosidosis, generalized GM1, type II) - GEIMM
IGF059/80 (human, Caucasian, Fanconi anemia, type I) - GEIMM
IGF059/82 (human, Caucasian, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF059/83 (human, Caucasian) - GEIMM
IGF059/84 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF059/85 (human, Caucasian) - GEIMM
IGF059/86 (human, Caucasian) - GEIMM
IGF059/87 (human, Caucasian) - GEIMM
IGF059/89 (human, Caucasian) - GEIMM
IGF059/90 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF059/91 (human, Caucasian) - GEIMM
IGF059/92 (human, Caucasian) - GEIMM
IGF059/93 (human, Caucasian) - GEIMM
IGF059/95 (human, Caucasian) - GEIMM
IGF059/97 (human, Caucasian) - GEIMM
IGF060/78 (human, Caucasian, proteolipid protein, myelin) - GEIMM
IGF060/79 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF060/80 (human, Caucasian) - GEIMM
IGF060/81 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF060/82 (human, Caucasian, fibromatosis, juvenile hyaline) - GEIMM
IGF060/83 (human, Caucasian) - GEIMM
IGF060/84 (human, Caucasian, hyperglycinemia, nonketotic) - GEIMM
IGF060/86 (human, Caucasian, osteogenesis imperfecta) - GEIMM
IGF060/87 (human, Caucasian) - GEIMM
IGF060/88 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF060/89 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF060/90 (human, Caucasian) - GEIMM
IGF060/91 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF060/92 (human, Caucasian) - GEIMM
IGF060/93 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF060/95 (human, Caucasian, homocystinuria - megaloblastic anemia) - GEIMM
IGF060/97 (human, Caucasian, Krabbe disease) - GEIMM
IGF061/76 (human, Caucasian) - GEIMM
IGF061/78 (human, Caucasian) - GEIMM
IGF061/79 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF061/81 (human, Caucasian, Hallervorden-Spatz disease) - GEIMM
IGF061/82 (human, Caucasian) - GEIMM
IGF061/83 (human, Caucasian) - GEIMM
IGF061/84 (human, Caucasian) - GEIMM
IGF061/85 (human, Caucasian, propionicacidemia I) - GEIMM
IGF061/86 (human, Caucasian) - GEIMM
IGF061/87 (human, Caucasian) - GEIMM
IGF061/88 (human, Caucasian) - GEIMM
IGF061/89 (human, Caucasian) - GEIMM
IGF061/90 (human, Caucasian) - GEIMM
IGF061/91 (human, Caucasian) - GEIMM
IGF061/92 (human, Caucasian) - GEIMM
IGF061/93 (human, Caucasian) - GEIMM
IGF061/95 (human, Caucasian, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF061/97 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF062/78 (human, Caucasian) - GEIMM
IGF062/79 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF062/81 (human, Caucasian) - GEIMM
IGF062/82 (human, Caucasian) - GEIMM
IGF062/83 (human, Caucasian) - GEIMM
IGF062/84 (human, Caucasian) - GEIMM
IGF062/85 (human, Caucasian, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF062/86 (human, Caucasian, osteogenesis imperfecta, type II) - GEIMM
IGF062/87 (human, Caucasian) - GEIMM
IGF062/88 (human, Caucasian) - GEIMM
IGF062/89 (human, Caucasian, neuraminidase deficiency with beta-galactosidase deficiency) - GEIMM
IGF062/90 (human, Caucasian, Costello syndrome) - GEIMM
IGF062/91 (human, Caucasian) - GEIMM
IGF062/95 (human, Caucasian, Glutaricacidemia I) - GEIMM
IGF062/97 (human, Caucasian) - GEIMM
IGF063/76 (human, Caucasian) - GEIMM
IGF063/77 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF063/78 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF063/79 (human, Caucasian) - GEIMM
IGF063/80 (human, Caucasian) - GEIMM
IGF063/81 (human, Caucasian) - GEIMM
IGF063/82 (human, Caucasian) - GEIMM
IGF063/84 (human, Caucasian) - GEIMM
IGF063/85 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF063/86 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF063/87 (human, Caucasian) - GEIMM
IGF063/90 (human, Caucasian) - GEIMM
IGF063/91 (human, Caucasian) - GEIMM
IGF063/93 (human, Caucasian) - GEIMM
IGF063/95 (human, Caucasian, homocystinuria - megaloblastic anemia) - GEIMM
IGF063/96 (human, Caucasian) - GEIMM
IGF064/76 (human, Caucasian) - GEIMM
IGF064/78 (human, Caucasian) - GEIMM
IGF064/79 (human, Caucasian) - GEIMM
IGF064/80 (human, Caucasian) - GEIMM
IGF064/81 (human, Caucasian, Wilson disease) - GEIMM
IGF064/82 (human, Caucasian) - GEIMM
IGF064/83 (human, Caucasian) - GEIMM
IGF064/84 (human, Caucasian) - GEIMM
IGF064/85 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF064/86 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF064/87 (human, Caucasian) - GEIMM
IGF064/88 (human, Caucasian) - GEIMM
IGF064/89 (human, Caucasian) - GEIMM
IGF064/90 (human, Caucasian) - GEIMM
IGF064/91 (human, Caucasian) - GEIMM
IGF064/93 (human, Caucasian) - GEIMM
IGF064/95 (human, Caucasian) - GEIMM
IGF065/77 (human, Caucasian) - GEIMM
IGF065/79 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF065/80 (human, Caucasian) - GEIMM
IGF065/81 (human, Caucasian) - GEIMM
IGF065/83 (human, Caucasian) - GEIMM
IGF065/84 (human, Caucasian) - GEIMM
IGF065/86 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF065/87 (human, Caucasian) - GEIMM
IGF065/88 (human, Caucasian, osteogenesis imperfecta) - GEIMM
IGF065/90 (human, Caucasian, testicular feminization syndrome) - GEIMM
IGF065/91 (human, Caucasian, Ehlers-Danlos syndrome) - GEIMM
IGF065/92 (human, Caucasian, Sjogren-Larsson syndrome) - GEIMM
IGF065/93 (human, Caucasian, mitochondrial respiratory chain complex I) - GEIMM
IGF065/95 (human, Caucasian) - GEIMM
IGF066/76 (human, Caucasian) - GEIMM
IGF066/77 (human, Caucasian) - GEIMM
IGF066/78 (human, Caucasian) - GEIMM
IGF066/79 (human, Caucasian) - GEIMM
IGF066/80 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF066/82 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF066/83 (human, Caucasian) - GEIMM
IGF066/84 (human, Caucasian, homocystinuria) - GEIMM
IGF066/85 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF066/86 (human, Caucasian) - GEIMM
IGF066/87 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF066/88 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF066/89 (human, Caucasian) - GEIMM
IGF066/90 (human, Caucasian, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF066/91 (human, Caucasian, carboydrate deficient glycoprotein syndrome, type I) - GEIMM
IGF066/92 (human, Caucasian) - GEIMM
IGF066/93 (human, Caucasian) - GEIMM
IGF066/95 (human, Caucasian) - GEIMM
IGF067/78 (human, Caucasian) - GEIMM
IGF067/81 (human, Caucasian) - GEIMM
IGF067/82 (human, Caucasian, methylmalonicacidemia) - GEIMM
IGF067/83 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF067/84 (human, Caucasian, arsa pseudodeficiency) - GEIMM
IGF067/85 (human, Caucasian) - GEIMM
IGF067/86 (human, Caucasian) - GEIMM
IGF067/87 (human, Caucasian, arthrogryposis multiplex congenita) - GEIMM
IGF067/88 (human, Caucasian) - GEIMM
IGF067/89 (human, Caucasian) - GEIMM
IGF067/90 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF067/91 (human, Caucasian, Zellweger syndrome) - GEIMM
IGF067/92 (human, Caucasian) - GEIMM
IGF067/93 (human, Caucasian) - GEIMM
IGF067/95 (human, Caucasian) - GEIMM
IGF068/78 (human, Caucasian) - GEIMM
IGF068/79 (human, Caucasian, cystic fibrosis) - GEIMM
IGF068/80 (human, Caucasian) - GEIMM
IGF068/82 (human, Caucasian, Aldrich syndrome) - GEIMM
IGF068/83 (human, Caucasian, Niemann-Pick disease, type B) - GEIMM
IGF068/84 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF068/85 (human, Caucasian) - GEIMM
IGF068/86 (human, Caucasian) - GEIMM
IGF068/87 (human, Caucasian) - GEIMM
IGF068/88 (human, Caucasian) - GEIMM
IGF068/89 (human, Caucasian, post-traumatic osteoporosis) - GEIMM
IGF068/90 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF068/91 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF068/92 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF068/93 (human, Caucasian) - GEIMM
IGF068/95 (human, Caucasian) - GEIMM
IGF069/78 (human, Caucasian) - GEIMM
IGF069/80 (human, Caucasian) - GEIMM
IGF069/82 (human, Caucasian) - GEIMM
IGF069/84 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF069/85 (human, Caucasian) - GEIMM
IGF069/86 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF069/87 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF069/88 (human, Caucasian) - GEIMM
IGF069/89 (human, Caucasian) - GEIMM
IGF069/90 (human, Caucasian) - GEIMM
IGF069/91 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF069/92 (human, Caucasian) - GEIMM
IGF069/93 (human, Caucasian) - GEIMM
IGF069/95 (human, Caucasian) - GEIMM
IGF070/76 (human, Caucasian) - GEIMM
IGF070/78 (human, Caucasian) - GEIMM
IGF070/80 (human, Caucasian) - GEIMM
IGF070/81 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF070/82 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF070/83 (human, Caucasian, Gaucher disease type III) - GEIMM
IGF070/84 (human, Caucasian) - GEIMM
IGF070/85 (human, Caucasian) - GEIMM
IGF070/86 (human, Caucasian, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF070/87 (human, Caucasian, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF070/88 (human, Caucasian, pyruvate dehydrogenase def.) - GEIMM
IGF070/89 (human, Caucasian, Edwards' syndrome / trisomy 18) - GEIMM
IGF070/90 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF070/91 (human, Caucasian) - GEIMM
IGF070/92 (human, Caucasian) - GEIMM
IGF070/93 (human, Caucasian) - GEIMM
IGF070/95 (human, Caucasian) - GEIMM
IGF071/76 (human, Caucasian) - GEIMM
IGF071/78 (human, Caucasian, Turner syndrome/noonan syndrome 1) - GEIMM
IGF071/80 (human, Caucasian) - GEIMM
IGF071/81 (human, Caucasian) - GEIMM
IGF071/82 (human, Caucasian) - GEIMM
IGF071/83 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF071/84 (human, Caucasian) - GEIMM
IGF071/85 (human, Caucasian, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF071/86 (human, Caucasian) - GEIMM
IGF071/87 (human, Caucasian) - GEIMM
IGF071/88 (human, Caucasian) - GEIMM
IGF071/89 (human, Caucasian, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF071/90 (human, Caucasian) - GEIMM
IGF071/92 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF071/93 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF071/95 (human, Caucasian, metachromatic leukodystrophy) - GEIMM
IGF072/76 (human, Caucasian) - GEIMM
IGF072/77 (human, Caucasian) - GEIMM
IGF072/78 (human, Caucasian) - GEIMM
IGF072/81 (human, Caucasian) - GEIMM
IGF072/82 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF072/83 (human, Caucasian, homocystinuria) - GEIMM
IGF072/84 (human, Caucasian) - GEIMM
IGF072/85 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF072/86 (human, Caucasian) - GEIMM
IGF072/87 (human, Caucasian) - GEIMM
IGF072/88 (human, Caucasian) - GEIMM
IGF072/89 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF072/90 (human, Caucasian) - GEIMM
IGF072/91 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF072/92 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF072/95 (human, Caucasian, mucolipidosis II) - GEIMM
IGF073/76 (human, Caucasian) - GEIMM
IGF073/78 (human, Caucasian) - GEIMM
IGF073/82 (human, Caucasian) - GEIMM
IGF073/83 (human, Caucasian) - GEIMM
IGF073/84 (human, Caucasian) - GEIMM
IGF073/85 (human, Caucasian, Turner syndrome/noonan syndrome 1) - GEIMM
IGF073/86 (human, Caucasian) - GEIMM
IGF073/87 (human, Caucasian) - GEIMM
IGF073/88 (human, Caucasian) - GEIMM
IGF073/89 (human, Caucasian) - GEIMM
IGF073/90 (human, Caucasian, mucolipidosis II) - GEIMM
IGF073/91 (human, Caucasian, geroderma osteodysplastica) - GEIMM
IGF073/92 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF073/95 (human, Caucasian, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF074/76 (human, Caucasian, triglyceride storage disease) - GEIMM
IGF074/78 (human, Caucasian, Laurence-Moon syndrome) - GEIMM
IGF074/79 (human, Caucasian) - GEIMM
IGF074/81 (human, Caucasian) - GEIMM
IGF074/82 (human, Caucasian) - GEIMM
IGF074/83 (human, Caucasian) - GEIMM
IGF074/84 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF074/86 (human, Caucasian) - GEIMM
IGF074/87 (human, Caucasian) - GEIMM
IGF074/88 (human, Caucasian) - GEIMM
IGF074/89 (human, Caucasian, Ellis-Van Creveld syndrome) - GEIMM
IGF074/90 (human, Caucasian) - GEIMM
IGF074/92 (human, Caucasian, Cockayne syndrome) - GEIMM
IGF075/76 (human, Caucasian) - GEIMM
IGF075/77 (human, Caucasian) - GEIMM
IGF075/78 (human, Caucasian, aspartylglycosaminuria) - GEIMM
IGF075/80 (human, Caucasian, sulfatidosis, juvenile, Austin type) - GEIMM
IGF075/81 (human, Caucasian, Krabbe disease) - GEIMM
IGF075/82 (human, Caucasian, mucopolysaccharidosis type III C) - GEIMM
IGF075/84 (human, Caucasian) - GEIMM
IGF075/86 (human, Caucasian, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF075/87 (human, Caucasian) - GEIMM
IGF075/88 (human, Caucasian) - GEIMM
IGF075/89 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF075/90 (human, Caucasian) - GEIMM
IGF075/91 (human, Caucasian) - GEIMM
IGF075/95 (human, Caucasian) - GEIMM
IGF076/76 (human, Caucasian) - GEIMM
IGF076/78 (human, Caucasian) - GEIMM
IGF076/79 (human, Caucasian) - GEIMM
IGF076/81 (human, Caucasian) - GEIMM
IGF076/82 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF076/83 (human, Caucasian) - GEIMM
IGF076/84 (human, Caucasian, dystonia musculorum deformans 2) - GEIMM
IGF076/85 (human, Caucasian) - GEIMM
IGF076/87 (human, Caucasian) - GEIMM
IGF076/89 (human, Caucasian, Smith-McCort dwarfism) - GEIMM
IGF076/90 (human, Caucasian) - GEIMM
IGF076/91 (human, Caucasian, Menkes syndrome) - GEIMM
IGF076/92 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF076/95 (human, Caucasian) - GEIMM
IGF077/76 (human, Caucasian) - GEIMM
IGF077/77 (human, Caucasian) - GEIMM
IGF077/78 (human, Caucasian) - GEIMM
IGF077/79 (human, Caucasian) - GEIMM
IGF077/80 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF077/81 (human, Caucasian, Krabbe disease) - GEIMM
IGF077/83 (human, Caucasian) - GEIMM
IGF077/84 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF077/85 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF077/86 (human, Caucasian) - GEIMM
IGF077/87 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF077/88 (human, Caucasian, Sandhoff disease) - GEIMM
IGF077/89 (human, Caucasian, mucolipidosis III) - GEIMM
IGF077/91 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF077/92 (human, Caucasian, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF077/95 (human, Caucasian) - GEIMM
IGF078/78 (human, Caucasian) - GEIMM
IGF078/79 (human, Caucasian) - GEIMM
IGF078/80 (human, Caucasian) - GEIMM
IGF078/81 (human, Caucasian) - GEIMM
IGF078/83 (human, Caucasian) - GEIMM
IGF078/84 (human, Caucasian, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF078/85 (human, Caucasian) - GEIMM
IGF078/86 (human, Caucasian) - GEIMM
IGF078/87 (human, Caucasian) - GEIMM
IGF078/89 (human, Caucasian, mucolipidosis II) - GEIMM
IGF078/90 (human, Caucasian) - GEIMM
IGF078/91 (human, Caucasian) - GEIMM
IGF078/92 (human, Caucasian) - GEIMM
IGF078/95 (human, Caucasian) - GEIMM
IGF079/76 (human, Caucasian, Ehlers-Danlos syndrome) - GEIMM
IGF079/77 (human, Caucasian) - GEIMM
IGF079/78 (human, Caucasian, spondyloepiphyseal dysplasia, congenital) - GEIMM
IGF079/80 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF079/81 (human, Caucasian) - GEIMM
IGF079/82 (human, Caucasian) - GEIMM
IGF079/83 (human, Caucasian) - GEIMM
IGF079/84 (human, Caucasian) - GEIMM
IGF079/86 (human, Caucasian) - GEIMM
IGF079/87 (human, Caucasian) - GEIMM
IGF079/89 (human, Caucasian, familial dolichocephaly) - GEIMM
IGF079/90 (human, Caucasian, early myoclonic encephalopathy) - GEIMM
IGF079/91 (human, Caucasian) - GEIMM
IGF080/76 (human, Caucasian, mucolipidosis III) - GEIMM
IGF080/78 (human, Caucasian) - GEIMM
IGF080/80 (human, Caucasian) - GEIMM
IGF080/81 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF080/82 (human, Caucasian) - GEIMM
IGF080/83 (human, Caucasian) - GEIMM
IGF080/84 (human, Caucasian) - GEIMM
IGF080/85 (human, Caucasian, glycogen storage disease III) - GEIMM
IGF080/86 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF080/87 (human, Caucasian) - GEIMM
IGF080/89 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF080/90 (human, Caucasian) - GEIMM
IGF080/91 (human, Caucasian) - GEIMM
IGF081/76 (human, Caucasian, mucolipidosis III) - GEIMM
IGF081/78 (human, Caucasian, mannosidosis, alpha b, lysosomal) - GEIMM
IGF081/80 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF081/81 (human, Caucasian, Menkes syndrome) - GEIMM
IGF081/82 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF081/83 (human, Caucasian) - GEIMM
IGF081/84 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF081/86 (human, Caucasian, diastrophic dysplasia) - GEIMM
IGF081/87 (human, Caucasian) - GEIMM
IGF081/89 (human, Caucasian, sudden infant death syndrome) - GEIMM
IGF081/90 (human, Caucasian, fucosidosis) - GEIMM
IGF081/91 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF081/92 (human, Caucasian, Sjogren-Larsson syndrome) - GEIMM
IGF082/76 (human, Caucasian, Farber lipogranulomatosis) - GEIMM
IGF082/80 (human, Caucasian) - GEIMM
IGF082/81 (human, Caucasian) - GEIMM
IGF082/82 (human, Caucasian) - GEIMM
IGF082/83 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF082/84 (human, Caucasian) - GEIMM
IGF082/85 (human, Caucasian) - GEIMM
IGF082/86 (human, Caucasian, mucolipidosis II) - GEIMM
IGF082/87 (human, Caucasian, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF082/89 (human, Caucasian) - GEIMM
IGF082/90 (human, Caucasian) - GEIMM
IGF082/91 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF082/92 (human, Caucasian) - GEIMM
IGF083/76 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF083/78 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF083/80 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF083/81 (human, Caucasian) - GEIMM
IGF083/82 (human, Caucasian, hyperglycinemia, nonketotic) - GEIMM
IGF083/83 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF083/84 (human, Caucasian, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF083/85 (human, Caucasian, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF083/86 (human, Caucasian) - GEIMM
IGF083/87 (human, Caucasian) - GEIMM
IGF083/89 (human, Caucasian) - GEIMM
IGF083/90 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF083/91 (human, Caucasian) - GEIMM
IGF083/92 (human, Caucasian) - GEIMM
IGF084/80 (human, Caucasian) - GEIMM
IGF084/81 (human, Caucasian) - GEIMM
IGF084/82 (human, Caucasian, gangliosidosis, generalized GM1, type II) - GEIMM
IGF084/83 (human, Caucasian) - GEIMM
IGF084/84 (human, Caucasian) - GEIMM
IGF084/85 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF084/86 (human, Caucasian) - GEIMM
IGF084/89 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF084/90 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF084/91 (human, Caucasian, proteolipid protein, myelin) - GEIMM
IGF084/92 (human, Caucasian) - GEIMM
IGF085/78 (human, Caucasian) - GEIMM
IGF085/80 (human, Caucasian) - GEIMM
IGF085/82 (human, Caucasian) - GEIMM
IGF085/84 (human, Caucasian) - GEIMM
IGF085/85 (human, Caucasian) - GEIMM
IGF085/86 (human, Caucasian, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF085/89 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF085/90 (human, Caucasian, Krabbe disease) - GEIMM
IGF085/91 (human, Caucasian) - GEIMM
IGF085/92 (human, Caucasian) - GEIMM
IGF086/78 (human, Caucasian, Krabbe disease) - GEIMM
IGF086/79 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF086/80 (human, Caucasian) - GEIMM
IGF086/84 (human, Caucasian) - GEIMM
IGF086/85 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF086/86 (human, Caucasian) - GEIMM
IGF086/89 (human, Caucasian) - GEIMM
IGF086/90 (human, Caucasian, Lesch-Nyhan syndrome) - GEIMM
IGF086/91 (human, Caucasian, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF086/92 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF087/78 (human, Caucasian) - GEIMM
IGF087/79 (human, Caucasian, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF087/80 (human, Caucasian) - GEIMM
IGF087/81 (human, Caucasian) - GEIMM
IGF087/82 (human, Caucasian) - GEIMM
IGF087/83 (human, Caucasian, mucolipidosis II) - GEIMM
IGF087/84 (human, Caucasian) - GEIMM
IGF087/85 (human, Caucasian) - GEIMM
IGF087/86 (human, Caucasian) - GEIMM
IGF087/87 (human, Caucasian) - GEIMM
IGF087/89 (human, Caucasian) - GEIMM
IGF087/91 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF087/92 (human, Caucasian, spongy degeneration of central nervous system /Canavan disease) - GEIMM
IGF088/78 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF088/79 (human, Caucasian) - GEIMM
IGF088/82 (human, Caucasian) - GEIMM
IGF088/83 (human, Caucasian) - GEIMM
IGF088/84 (human, Caucasian) - GEIMM
IGF088/86 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF088/87 (human, Caucasian) - GEIMM
IGF088/89 (human, Caucasian) - GEIMM
IGF088/90 (human, Caucasian) - GEIMM
IGF088/91 (human, Caucasian) - GEIMM
IGF088/92 (human, Caucasian) - GEIMM
IGF089/78 (human, Caucasian) - GEIMM
IGF089/79 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF089/80 (human, Caucasian, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF089/81 (human, Caucasian) - GEIMM
IGF089/82 (human, Caucasian, frontometaphyseal dysplasia) - GEIMM
IGF089/83 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF089/84 (human, Caucasian) - GEIMM
IGF089/85 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF089/87 (human, Caucasian, osteogenesis imperfecta, type II) - GEIMM
IGF089/89 (human, Caucasian, osteogenesis imperfecta, type II) - GEIMM
IGF089/90 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF089/91 (human, Caucasian) - GEIMM
IGF089/92 (human, Caucasian) - GEIMM
IGF090/78 (human, Caucasian, Laurence-Moon syndrome) - GEIMM
IGF090/79 (human, Caucasian) - GEIMM
IGF090/82 (human, Caucasian) - GEIMM
IGF090/83 (human, Caucasian) - GEIMM
IGF090/84 (human, Caucasian) - GEIMM
IGF090/86 (human, Caucasian, Larsen syndrome) - GEIMM
IGF090/87 (human, Caucasian, osteogenesis imperfecta) - GEIMM
IGF090/89 (human, Caucasian) - GEIMM
IGF090/91 (human, Caucasian, carboydrate deficient glycoprotein syndrome, type I) - GEIMM
IGF090/92 (human, Caucasian) - GEIMM
IGF091/78 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF091/79 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF091/81 (human, Caucasian) - GEIMM
IGF091/82 (human, Caucasian, mucolipidosis II) - GEIMM
IGF091/83 (human, Caucasian) - GEIMM
IGF091/84 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF091/85 (human, Caucasian, argininosuccinicaciduria) - GEIMM
IGF091/86 (human, Caucasian, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF091/87 (human, Caucasian) - GEIMM
IGF091/89 (human, Caucasian) - GEIMM
IGF091/92 (human, Caucasian) - GEIMM
IGF092/78 (human, Caucasian) - GEIMM
IGF092/82 (human, Caucasian, phenylketonuria I) - GEIMM
IGF092/83 (human, Caucasian) - GEIMM
IGF092/84 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF092/86 (human, Caucasian) - GEIMM
IGF092/87 (human, Caucasian) - GEIMM
IGF093/78 (human, Caucasian) - GEIMM
IGF093/80 (human, Caucasian) - GEIMM
IGF093/81 (human, Caucasian) - GEIMM
IGF093/82 (human, Caucasian) - GEIMM
IGF093/83 (human, Caucasian) - GEIMM
IGF093/84 (human, Caucasian) - GEIMM
IGF093/85 (human, Caucasian, osteogenesis imperfecta) - GEIMM
IGF093/86 (human, Caucasian, mucolipidosis II) - GEIMM
IGF093/87 (human, Caucasian, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF093/89 (human, Caucasian, osteogenesis imperfecta, type IV) - GEIMM
IGF093/90 (human, Caucasian) - GEIMM
IGF093/91 (human, Caucasian, Krabbe disease) - GEIMM
IGF093/92 (human, Caucasian) - GEIMM
IGF094/78 (human, Caucasian, arsa pseudodeficiency) - GEIMM
IGF094/80 (human, Caucasian) - GEIMM
IGF094/81 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF094/83 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF094/84 (human, Caucasian) - GEIMM
IGF094/85 (human, Caucasian) - GEIMM
IGF094/86 (human, Caucasian) - GEIMM
IGF094/87 (human, Caucasian) - GEIMM
IGF094/89 (human, Caucasian) - GEIMM
IGF094/90 (human, Caucasian) - GEIMM
IGF094/91 (human, Caucasian) - GEIMM
IGF094/92 (human, Caucasian, homocystinuria - megaloblastic anemia) - GEIMM
IGF095/78 (human, Caucasian) - GEIMM
IGF095/79 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF095/80 (human, Caucasian) - GEIMM
IGF095/82 (human, Caucasian) - GEIMM
IGF095/83 (human, Caucasian) - GEIMM
IGF095/85 (human, Caucasian, Shwachman-Bodian syndrome) - GEIMM
IGF095/86 (human, Caucasian, Krabbe disease) - GEIMM
IGF095/87 (human, Caucasian) - GEIMM
IGF095/89 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF095/91 (human, Caucasian) - GEIMM
IGF096/78 (human, Caucasian) - GEIMM
IGF096/79 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF096/80 (human, Caucasian) - GEIMM
IGF096/81 (human, Caucasian) - GEIMM
IGF096/82 (human, Caucasian, Ehlers-Danlos syndrome) - GEIMM
IGF096/83 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF096/84 (human, Caucasian, camptomelic dwarfism) - GEIMM
IGF096/85 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF096/86 (human, Caucasian) - GEIMM
IGF096/90 (human, Caucasian) - GEIMM
IGF096/91 (human, Caucasian) - GEIMM
IGF096/92 (human, Caucasian) - GEIMM
IGF097/78 (human, Caucasian) - GEIMM
IGF097/79 (human, Caucasian) - GEIMM
IGF097/80 (human, Caucasian) - GEIMM
IGF097/81 (human, Caucasian) - GEIMM
IGF097/82 (human, Caucasian) - GEIMM
IGF097/83 (human, Caucasian) - GEIMM
IGF097/84 (human, Caucasian) - GEIMM
IGF097/85 (human, Caucasian) - GEIMM
IGF097/86 (human, Caucasian, Gaucher disease type III) - GEIMM
IGF097/87 (human, Caucasian) - GEIMM
IGF097/89 (human, Caucasian, cri du chat syndrome) - GEIMM
IGF097/90 (human, Caucasian, spastic paraparesis) - GEIMM
IGF097/92 (human, Caucasian) - GEIMM
IGF098/78 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF098/79 (human, Caucasian) - GEIMM
IGF098/80 (human, Caucasian) - GEIMM
IGF098/82 (human, Caucasian) - GEIMM
IGF098/83 (human, Caucasian) - GEIMM
IGF098/84 (human, Caucasian) - GEIMM
IGF098/85 (human, Caucasian) - GEIMM
IGF098/86 (human, Caucasian, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF098/87 (human, Caucasian) - GEIMM
IGF098/89 (human, South American, mucolipidosis II) - GEIMM
IGF098/90 (human, Caucasian) - GEIMM
IGF098/92 (human, Caucasian, glyceronephosphate o-acyltransferase) - GEIMM
IGF099/78 (human, Caucasian) - GEIMM
IGF099/79 (human, Caucasian, adrenal hyperplasia III) - GEIMM
IGF099/80 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF099/82 (human, Caucasian) - GEIMM
IGF099/83 (human, Caucasian) - GEIMM
IGF099/84 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF099/85 (human, Caucasian) - GEIMM
IGF099/86 (human, Caucasian, fibrodysplasia ossificans progressiva) - GEIMM
IGF099/87 (human, Caucasian) - GEIMM
IGF099/89 (human, Caucasian) - GEIMM
IGF099/90 (human, Caucasian, spinal muscolar atrophy III) - GEIMM
IGF099/92 (human, Caucasian) - GEIMM
IGF100/78 (human, Caucasian, mucopolysaccharidosis type VI) - GEIMM
IGF100/79 (human, Caucasian) - GEIMM
IGF100/80 (human, Caucasian) - GEIMM
IGF100/81 (human, Caucasian, porphiria, acute intermittent) - GEIMM
IGF100/83 (human, Caucasian) - GEIMM
IGF100/84 (human, Caucasian) - GEIMM
IGF100/85 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF100/86 (human, Caucasian) - GEIMM
IGF100/87 (human, Caucasian) - GEIMM
IGF100/89 (human, Caucasian, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF100/90 (human, Caucasian, osteogenesis imperfecta) - GEIMM
IGF100/91 (human, Caucasian, articular hypermobility syndrome) - GEIMM
IGF100/92 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF101/78 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF101/79 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF101/80 (human, Caucasian, homocystinuria) - GEIMM
IGF101/81 (human, Caucasian, trichothiodystrophy) - GEIMM
IGF101/82 (human, Caucasian) - GEIMM
IGF101/83 (human, Caucasian, mucopolysaccharidosis type III C) - GEIMM
IGF101/84 (human, Caucasian) - GEIMM
IGF101/85 (human, Caucasian) - GEIMM
IGF101/86 (human, Caucasian) - GEIMM
IGF101/89 (human, Caucasian) - GEIMM
IGF101/90 (human, Caucasian) - GEIMM
IGF101/91 (human, Caucasian, Marfan syndrome) - GEIMM
IGF102/78 (human, Caucasian, neuraminidase deficiency) - GEIMM
IGF102/80 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF102/82 (human, Caucasian) - GEIMM
IGF102/83 (human, Caucasian, hyperlipoproteinemia I) - GEIMM
IGF102/84 (human, Caucasian) - GEIMM
IGF102/85 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF102/86 (human, Caucasian) - GEIMM
IGF102/87 (human, Caucasian) - GEIMM
IGF102/89 (human, Caucasian, trisomy 21 / Down syndrome) - GEIMM
IGF102/90 (human, Caucasian) - GEIMM
IGF102/91 (human, Caucasian, Marfan syndrome) - GEIMM
IGF103/79 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF103/81 (human, Caucasian, propionicacidemia I) - GEIMM
IGF103/82 (human, Caucasian) - GEIMM
IGF103/84 (human, Caucasian) - GEIMM
IGF103/85 (human, Caucasian) - GEIMM
IGF103/86 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF103/89 (human, Caucasian) - GEIMM
IGF103/90 (human, Caucasian) - GEIMM
IGF103/91 (human, Caucasian, Marfan syndrome) - GEIMM
IGF104/78 (human, Caucasian, gangliosidosis, generalized GM1, type II) - GEIMM
IGF104/79 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF104/81 (human, Caucasian, maple syrup urine disease) - GEIMM
IGF104/82 (human, Caucasian, Lesch-Nyhan syndrome) - GEIMM
IGF104/83 (human, Caucasian) - GEIMM
IGF104/84 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF104/85 (human, Caucasian) - GEIMM
IGF104/89 (human, Caucasian) - GEIMM
IGF104/90 (human, Caucasian) - GEIMM
IGF104/91 (human, Caucasian) - GEIMM
IGF105/80 (human, Caucasian) - GEIMM
IGF105/81 (human, Caucasian, fucosidosis) - GEIMM
IGF105/82 (human, Caucasian) - GEIMM
IGF105/83 (human, Caucasian) - GEIMM
IGF105/84 (human, Caucasian) - GEIMM
IGF105/85 (human, Caucasian, Lowe oculocerebrorenal syndrome) - GEIMM
IGF105/87 (human, Caucasian) - GEIMM
IGF105/89 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGF105/91 (human, Caucasian) - GEIMM
IGF106/78 (human, Caucasian) - GEIMM
IGF106/79 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF106/80 (human, Caucasian) - GEIMM
IGF106/81 (human, Caucasian) - GEIMM
IGF106/82 (human, Caucasian) - GEIMM
IGF106/83 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF106/84 (human, Caucasian) - GEIMM
IGF106/85 (human, Caucasian) - GEIMM
IGF106/90 (human, Caucasian) - GEIMM
IGF106/91 (human, Caucasian, mucopolysaccharidosis type III C) - GEIMM
IGF107/80 (human, Caucasian) - GEIMM
IGF107/81 (human, Caucasian, fructose intolerance, hereditary) - GEIMM
IGF107/82 (human, Caucasian, Bardet-Biedl syndrome) - GEIMM
IGF107/83 (human, Caucasian) - GEIMM
IGF107/84 (human, Caucasian, glycogen storage disease III) - GEIMM
IGF107/85 (human, Caucasian) - GEIMM
IGF107/89 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF107/90 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF107/91 (human, Caucasian) - GEIMM
IGF108/80 (human, Caucasian) - GEIMM
IGF108/81 (human, Caucasian, Gaucher disease type III) - GEIMM
IGF108/82 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF108/83 (human, Caucasian, hyperammonemia due to carbamoylphosphate synthetase deficien.) - GEIMM
IGF108/84 (human, Caucasian) - GEIMM
IGF108/85 (human, Caucasian) - GEIMM
IGF108/90 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF108/91 (human, Caucasian, methylmalonicacidemia) - GEIMM
IGF109/79 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF109/80 (human, Caucasian) - GEIMM
IGF109/81 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF109/83 (human, Caucasian) - GEIMM
IGF109/84 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF109/85 (human, Caucasian, Laurence-Moon syndrome) - GEIMM
IGF109/91 (human, Caucasian, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF110/78 (human, Caucasian, homocystinuria) - GEIMM
IGF110/80 (human, Caucasian) - GEIMM
IGF110/81 (human, Caucasian) - GEIMM
IGF110/82 (human, Caucasian, glycogen storage disease I) - GEIMM
IGF110/83 (human, Caucasian) - GEIMM
IGF110/85 (human, Caucasian, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF110/91 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF111/80 (human, Caucasian, mucopolysaccharidosis type VI) - GEIMM
IGF111/82 (human, Caucasian) - GEIMM
IGF111/83 (human, Caucasian, galactose epimerase deficiency) - GEIMM
IGF111/84 (human, Caucasian) - GEIMM
IGF111/85 (human, Caucasian) - GEIMM
IGF111/90 (human, Caucasian) - GEIMM
IGF112/80 (human, Caucasian) - GEIMM
IGF112/81 (human, Caucasian) - GEIMM
IGF112/82 (human, Caucasian, maple syrup urine disease) - GEIMM
IGF112/83 (human, Caucasian) - GEIMM
IGF112/84 (human, Caucasian) - GEIMM
IGF112/85 (human, Caucasian, gangliosidosis, generalized GM1, type II) - GEIMM
IGF112/87 (human, Caucasian) - GEIMM
IGF112/91 (human, Caucasian) - GEIMM
IGF113/80 (human, Caucasian, Gaucher disease type II) - GEIMM
IGF113/81 (human, Caucasian, methylmalonicacidemia) - GEIMM
IGF113/82 (human, Caucasian) - GEIMM
IGF113/83 (human, Caucasian, Berardinelli syndrome /seip syndrome) - GEIMM
IGF113/84 (human, Caucasian) - GEIMM
IGF113/85 (human, Caucasian, Marfan syndrome) - GEIMM
IGF113/87 (human, Caucasian) - GEIMM
IGF113/91 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGF114/82 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF114/83 (human, Caucasian) - GEIMM
IGF114/84 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF114/85 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF114/87 (human, Caucasian) - GEIMM
IGF114/91 (human, Caucasian) - GEIMM
IGF115/81 (human, Caucasian) - GEIMM
IGF115/82 (human, Caucasian) - GEIMM
IGF115/83 (human, Caucasian) - GEIMM
IGF115/84 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF115/85 (human, Caucasian) - GEIMM
IGF115/90 (human, Caucasian, leprechaunism) - GEIMM
IGF115/91 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF116/81 (human, Caucasian) - GEIMM
IGF116/82 (human, Caucasian, Gaucher disease type II) - GEIMM
IGF116/83 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF116/84 (human, Caucasian) - GEIMM
IGF116/85 (human, Caucasian) - GEIMM
IGF116/91 (human, Caucasian) - GEIMM
IGF117/80 (human, Caucasian) - GEIMM
IGF117/81 (human, Caucasian) - GEIMM
IGF117/83 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF117/84 (human, Caucasian, fibrodysplasia ossificans progressiva) - GEIMM
IGF117/85 (human, Caucasian, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF117/91 (human, Caucasian, osteogenesis imperfecta) - GEIMM
IGF118/80 (human, Caucasian, glycogen storage disease II) - GEIMM
IGF118/81 (human, Caucasian, mucolipidosis II) - GEIMM
IGF118/82 (human, Caucasian) - GEIMM
IGF118/84 (human, Caucasian) - GEIMM
IGF118/85 (human, Caucasian) - GEIMM
IGF118/91 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGF119/83 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF119/84 (human, Caucasian) - GEIMM
IGF119/85 (human, Caucasian) - GEIMM
IGF119/91 (human, Caucasian) - GEIMM
IGF120/81 (human, Caucasian, maple syrup urine disease) - GEIMM
IGF120/82 (human, Caucasian) - GEIMM
IGF120/83 (human, Caucasian, triglyceride storage disease) - GEIMM
IGF120/84 (human, Caucasian, fucosidosis) - GEIMM
IGF120/85 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF120/91 (human, Caucasian) - GEIMM
IGF121/80 (human, Caucasian) - GEIMM
IGF121/82 (human, Caucasian) - GEIMM
IGF121/83 (human, Caucasian) - GEIMM
IGF121/84 (human, Caucasian) - GEIMM
IGF121/85 (human, Caucasian) - GEIMM
IGF121/91 (human, Caucasian, mucopolysaccharidosis type III C) - GEIMM
IGF122/82 (human, Caucasian) - GEIMM
IGF122/83 (human, Caucasian) - GEIMM
IGF122/84 (human, Caucasian, Turner syndrome/noonan syndrome 1) - GEIMM
IGF122/85 (human, Caucasian) - GEIMM
IGF122/91 (human, Caucasian, pyruvate dehydrogenase def.) - GEIMM
IGF123/80 (human, Caucasian) - GEIMM
IGF123/81 (human, Caucasian) - GEIMM
IGF123/82 (human, Caucasian) - GEIMM
IGF123/83 (human, Caucasian) - GEIMM
IGF123/84 (human, Caucasian) - GEIMM
IGF123/85 (human, Caucasian) - GEIMM
IGF123/91 (human, Caucasian, Krabbe disease) - GEIMM
IGF124/80 (human, Caucasian) - GEIMM
IGF124/81 (human, Caucasian, xeroderma pigmentosum I) - GEIMM
IGF124/82 (human, Caucasian, Jarcho-Levin syndrome) - GEIMM
IGF124/84 (human, Caucasian, Sandhoff disease) - GEIMM
IGF124/85 (human, Caucasian) - GEIMM
IGF124/91 (human, Caucasian) - GEIMM
IGF125/80 (human, Caucasian) - GEIMM
IGF125/81 (human, Caucasian, xeroderma pigmentosum I) - GEIMM
IGF125/82 (human, Caucasian, dibasicaminoaciduria II) - GEIMM
IGF125/84 (human, Caucasian, fibrodysplasia ossificans progressiva) - GEIMM
IGF125/85 (human, Caucasian) - GEIMM
IGF126/80 (human, Caucasian) - GEIMM
IGF126/81 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF126/83 (human, Caucasian) - GEIMM
IGF126/84 (human, Caucasian) - GEIMM
IGF126/85 (human, Caucasian) - GEIMM
IGF126/91 (human, Caucasian, congenital undergrowth of left leg) - GEIMM
IGF127/80 (human, Caucasian) - GEIMM
IGF127/82 (human, Caucasian, Alexander disease) - GEIMM
IGF127/83 (human, Caucasian) - GEIMM
IGF127/85 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF127/91 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGF128/80 (human, Caucasian) - GEIMM
IGF128/83 (human, Caucasian) - GEIMM
IGF128/84 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF128/85 (human, Caucasian) - GEIMM
IGF128/91 (human, Caucasian, adrenal gland tumor) - GEIMM
IGF129/80 (human, Caucasian, mucopolysaccharidosis type VI) - GEIMM
IGF129/82 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF129/84 (human, Caucasian) - GEIMM
IGF130/82 (human, Caucasian, tyrosine transaminase deficiency) - GEIMM
IGF130/83 (human, Caucasian, Lesch-Nyhan syndrome) - GEIMM
IGF130/84 (human, Caucasian) - GEIMM
IGF130/91 (human, Caucasian, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF131/80 (human, Caucasian, propionicacidemia I) - GEIMM
IGF131/82 (human, Caucasian) - GEIMM
IGF131/83 (human, Caucasian, dystonia musculorum deformans 2) - GEIMM
IGF131/84 (human, Caucasian) - GEIMM
IGF132/80 (human, Caucasian, Charcot-Marie-Tooth disease) - GEIMM
IGF132/82 (human, Caucasian) - GEIMM
IGF132/83 (human, Caucasian) - GEIMM
IGF133/80 (human, Caucasian) - GEIMM
IGF133/82 (human, Caucasian) - GEIMM
IGF133/83 (human, Caucasian) - GEIMM
IGF134/82 (human, Caucasian, fucosidosis) - GEIMM
IGF134/83 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF135/80 (human, Caucasian) - GEIMM
IGF135/82 (human, Caucasian, spongy degeneration of central nervous system /Canavan disease) - GEIMM
IGF135/83 (human, Caucasian, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF136/80 (human, Caucasian) - GEIMM
IGF136/82 (human, Caucasian) - GEIMM
IGF136/83 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF137/80 (human, Caucasian, Charcot-Marie-Tooth disease) - GEIMM
IGF137/83 (human, Caucasian, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF138/80 (human, Caucasian) - GEIMM
IGF138/82 (human, Caucasian, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF138/83 (human, Caucasian) - GEIMM
IGF139/80 (human, Caucasian, Charcot-Marie-Tooth disease) - GEIMM
IGF139/83 (human, Caucasian) - GEIMM
IGF140/80 (human, Caucasian) - GEIMM
IGF140/83 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF141/80 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF141/82 (human, Caucasian, xerodermic idiocy of De Sanctis and Cacchione) - GEIMM
IGF141/83 (human, Caucasian, trisomy 21 / Down syndrome) - GEIMM
IGF142/80 (human, Caucasian, Gaucher disease type I) - GEIMM
IGF142/83 (human, Caucasian) - GEIMM
IGF143/80 (human, Caucasian) - GEIMM
IGF143/82 (human, Caucasian, phenylketonuria I) - GEIMM
IGF143/83 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF144/80 (human, Caucasian, cystic fibrosis) - GEIMM
IGF144/82 (human, Caucasian, phenylketonuria I) - GEIMM
IGF144/83 (human, Caucasian) - GEIMM
IGF145/80 (human, Caucasian) - GEIMM
IGF145/83 (human, Caucasian) - GEIMM
IGF146/80 (human, Caucasian, ornithine-transcarbamylase deficiency) - GEIMM
IGF146/82 (human, Caucasian, sialic acid storage disease) - GEIMM
IGF147/82 (human, Caucasian) - GEIMM
IGF147/83 (human, Caucasian) - GEIMM
IGF148/82 (human, Caucasian) - GEIMM
IGF148/83 (human, Caucasian) - GEIMM
IGF149/82 (human, Caucasian) - GEIMM
IGF149/83 (human, Caucasian, mucopolysaccharidosis type IV B / Morquio syndrome) - GEIMM
IGF150/83 (human, Caucasian) - GEIMM
IGF151/82 (human, Caucasian) - GEIMM
IGF151/83 (human, Caucasian) - GEIMM
IGF152/82 (human, Caucasian) - GEIMM
IGF152/83 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGF153/82 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF153/83 (human, Caucasian) - GEIMM
IGF154/82 (human, Caucasian) - GEIMM
IGF154/83 (human, Caucasian, glycogen storage disease III) - GEIMM
IGF155/82 (human, Caucasian) - GEIMM
IGF156/82 (human, Caucasian, xerodermic idiocy of De Sanctis and Cacchione) - GEIMM
IGF156/83 (human, Caucasian) - GEIMM
IGF157/82 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF157/83 (human, Caucasian) - GEIMM
IGF158/82 (human, Caucasian, sponastrime dysplasia) - GEIMM
IGF158/83 (human, Caucasian) - GEIMM
IGF159/82 (human, Caucasian) - GEIMM
IGF159/83 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF160/82 (human, Caucasian, Niemann-Pick disease, type B) - GEIMM
IGF160/83 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF161/83 (human, Caucasian, propionicacidemia I) - GEIMM
IGF162/83 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF163/83 (human, Caucasian, Gaucher disease type III) - GEIMM
IGF164/83 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGF165/83 (human, Caucasian) - GEIMM
IGF166/83 (human, Caucasian, trichothiodystrophy) - GEIMM
IGF168/83 (human, Caucasian) - GEIMM
IGF169/83 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGF170/83 (human, Caucasian) - GEIMM
IGF171/83 (human, Caucasian) - GEIMM
IGF172/83 (human, Caucasian) - GEIMM
IGF173/83 (human, Caucasian) - GEIMM
IGF174/83 (human, Caucasian) - GEIMM
IGF175/83 (human, Caucasian) - GEIMM
IGF176/83 (human, Caucasian) - GEIMM
IGF177/83 (human, Caucasian) - GEIMM
IGF178/83 (human, Caucasian) - GEIMM
IGF179/83 (human, Caucasian) - GEIMM
IGF180/83 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGF181/83 (human, Caucasian, mannosidosis, alpha b, lysosomal) - GEIMM
IGF182/83 (human, Caucasian, gangliosidosis, generalized GM1, type II) - GEIMM
IGF183/83 (human, Caucasian, Turner syndrome/noonan syndrome 1) - GEIMM
IGF186/83 (human, Caucasian) - GEIMM
IGF187/83 (human, Caucasian, hyperglycinemia, nonketotic) - GEIMM
IGF200/83 (human, Caucasian) - GEIMM
IGF201/83 (human, Caucasian) - GEIMM
IGF740/88 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IMG-1002 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-1003 (human, progeria syndrome) - MWCMG
IMG-1006 (human, osteogenesis imperfecta) - MWCMG
IMG-1007 (human, Krabbe disease) - MWCMG
IMG-1008 (human, Edwards' syndrome / trisomy 18) - MWCMG
IMG-1009 (human, Edwards' syndrome / trisomy 18) - MWCMG
IMG-1018 (human, Krabbe disease) - MWCMG
IMG-1019 (human, Krabbe disease) - MWCMG
IMG-1021 XP4MO (human, xeroderma pigmentosum) - MWCMG
IMG-1023 (human, Krabbe disease) - MWCMG
IMG-1024 XP5MO (human, xeroderma pigmentosum) - MWCMG
IMG-1025 (human, Prader-Willi syndrome) - MWCMG
IMG-1027 (human, basal cell nevus syndrome) - MWCMG
IMG-1028 XP6MO (human, xeroderma pigmentosum) - MWCMG
IMG-1032 (human, trisomy 21 / Down syndrome) - MWCMG
IMG-1035 (human, trisomy 21 / Down syndrome) - MWCMG
IMG-1036 (human, trisomy 21 / Down syndrome) - MWCMG
IMG-1037 (human) - MWCMG
IMG-1038 (human, trisomy 21 / Down syndrome) - MWCMG
IMG-1046 (human, triploidy) - MWCMG
IMG-1048 (human, poly-X syndrome) - MWCMG
IMG-1049 (human, poly-X syndrome) - MWCMG
IMG-1053 (human, osteogenesis imperfecta) - MWCMG
IMG-1054 (human, osteogenesis imperfecta) - MWCMG
IMG-1062 (human, triploidy) - MWCMG
IMG-1065 (human, Marfan syndrome) - MWCMG
IMG-1066 (human, Marfan syndrome) - MWCMG
IMG-1068 (human, triplo-X syndrome) - MWCMG
IMG-1069 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-1070 (human, triplo-X syndrome) - MWCMG
IMG-1080 XP7MO (human, xeroderma pigmentosum) - MWCMG
IMG-1106 (human, Cockayne syndrome) - MWCMG
IMG-1111 (human, Marfan syndrome) - MWCMG
IMG-1112 (human, metachromatic leukodystrophy) - MWCMG
IMG-1116 (human, metachromatic leukodystrophy) - MWCMG
IMG-1117 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-1119 (human, mucopolysaccharidosis type II) - MWCMG
IMG-1121 (human, metachromatic leukodystrophy) - MWCMG
IMG-1122 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-1123 (human, metachromatic leukodystrophy) - MWCMG
IMG-1124 (human, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-1126 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-1127 (human, mucopolysaccharidosis type II) - MWCMG
IMG-1129 (human, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-1132 (human, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-1134 (human, mucopolysaccharidosis type II) - MWCMG
IMG-1135 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-1136 (human, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-1137 (human, mucopolysaccharidosis type II) - MWCMG
IMG-1140 (human, Niemann-Pick disease) - MWCMG
IMG-1143 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-1144 (human, mucopolysaccharidosis type II) - MWCMG
IMG-1145 (human, mucopolysaccharidosis type II) - MWCMG
IMG-1146 (human, Gaucher disease) - MWCMG
IMG-1149 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-1154 (human, mucopolysaccharidosis type II) - MWCMG
IMG-1156 (human, mucolipidosis) - MWCMG
IMG-1161 (human, mucopolysaccharidosis type IV B / Morquio syndrome) - MWCMG
IMG-1163 (human, mucopolysaccharidosis type II) - MWCMG
IMG-1164 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-1165 (human, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-1176 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-1181 (human, neuraminidase deficiency) - MWCMG
IMG-1211 (human, triploidy) - MWCMG
IMG-1215 (human, Beckwith-Wiedemann syndrome) - MWCMG
IMG-1216 (human, retinoblastoma) - MWCMG
IMG-1217 XP8MO (human, xeroderma pigmentosum) - MWCMG
IMG-1230 (human, Down syndrome, mosaic) - MWCMG
IMG-1233 (human, amyloidosis) - MWCMG
IMG-1234 (human, amyloidosis) - MWCMG
IMG-1235 (human, amyloidosis) - MWCMG
IMG-1239 (human, Beckwith-Wiedemann syndrome) - MWCMG
IMG-1241 (human, Down syndrome, mosaic) - MWCMG
IMG-1247 XP9MO (human, xeroderma pigmentosum) - MWCMG
IMG-1250 (human, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-1266 (human, Down syndrome, mosaic) - MWCMG
IMG-1311 (human, Patau syndrome / trisomy 13) - MWCMG
IMG-1344 (human, Down syndrome, mosaic) - MWCMG
IMG-1347 (human, Down syndrome, mosaic) - MWCMG
IMG-1359 (human, YY-syndrome) - MWCMG
IMG-1360 (human, YY-syndrome) - MWCMG
IMG-1366 (human, Down syndrome, mosaic) - MWCMG
IMG-1370 (human, Dubowitz syndrome) - MWCMG
IMG-1371 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-1373 (human, Patau syndrome / trisomy 13) - MWCMG
IMG-1388 (human, Down syndrome, mosaic) - MWCMG
IMG-1401 (human, balanced chromosome translocation) - MWCMG
IMG-1402 (human, balanced chromosome translocation) - MWCMG
IMG-1403 (human, balanced chromosome translocation) - MWCMG
IMG-1404 (human, balanced chromosome translocation) - MWCMG
IMG-1407 (human, balanced chromosome translocation) - MWCMG
IMG-1408 (human, balanced chromosome translocation) - MWCMG
IMG-1409 (human, balanced chromosome translocation) - MWCMG
IMG-1410 (human, balanced chromosome translocation) - MWCMG
IMG-1413 (human, balanced chromosome translocation) - MWCMG
IMG-1414 (human, balanced chromosome translocation) - MWCMG
IMG-1415 (human, balanced chromosome translocation) - MWCMG
IMG-1416 (human, balanced chromosome translocation) - MWCMG
IMG-1417 (human, balanced chromosome translocation) - MWCMG
IMG-1418 (human, balanced chromosome translocation) - MWCMG
IMG-1419 (human, balanced chromosome translocation) - MWCMG
IMG-1420 (human, balanced chromosome translocation) - MWCMG
IMG-1421 (human, balanced chromosome translocation) - MWCMG
IMG-1425 (human, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-1432 (human, balanced chromosome translocation) - MWCMG
IMG-3003 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-375 (human, trisomy 21 / Down syndrome) - MWCMG
IMG-478 (human, triploidy) - MWCMG
IMG-484 XP2MO (human, xeroderma pigmentosum) - MWCMG
IMG-492 (human, YY-syndrome) - MWCMG
IMG-493 (human, poly-X syndrome) - MWCMG
IMG-608 (human, poly-X syndrome) - MWCMG
IMG-610 (human, Gaucher disease) - MWCMG
IMG-630 (human, Tay-Sachs disease) - MWCMG
IMG-636 (human, scleroderma, familial progressive) - MWCMG
IMG-638 XP3LE (human, pigmented xerodermoid) - MWCMG
IMG-639 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-649 (human, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-650 (human, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-653 (human, thalassemia) - MWCMG
IMG-655 (human, Niemann-Pick disease) - MWCMG
IMG-656 (human, Tay-Sachs disease) - MWCMG
IMG-667 XP2LE (human, xeroderma pigmentosum) - MWCMG
IMG-672 (human, xeroderma pigmentosum) - MWCMG
IMG-673 (human, xeroderma pigmentosum) - MWCMG
IMG-674 (human, xeroderma pigmentosum) - MWCMG
IMG-675 (human, xeroderma pigmentosum) - MWCMG
IMG-676 (human, xeroderma pigmentosum) - MWCMG
IMG-678 (human, Lesch-Nyhan syndrome) - MWCMG
IMG-679 (human, Lesch-Nyhan syndrome) - MWCMG
IMG-683 (human, Turner syndrome, mosaic) - MWCMG
IMG-688 (human, Turner syndrome, mosaic) - MWCMG
IMG-691 (human, Edwards' syndrome / trisomy 18) - MWCMG
IMG-694 (human, cri du chat syndrome) - MWCMG
IMG-695 (human, scleroderma, familial progressive) - MWCMG
IMG-706 (human, progeria syndrome) - MWCMG
IMG-707 (human, triploidy) - MWCMG
IMG-709 (human, testicular feminization syndrome) - MWCMG
IMG-711 (human, Tay-Sachs disease) - MWCMG
IMG-723 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-724 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-725 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-726 (human, Sandhoff disease) - MWCMG
IMG-728 (human, Sandhoff disease) - MWCMG
IMG-729 (human, Sandhoff disease) - MWCMG
IMG-730 XP3MO (human, xeroderma pigmentosum) - MWCMG
IMG-733 (human, osteogenesis imperfecta) - MWCMG
IMG-734 (human, trisomy 21 / Down syndrome) - MWCMG
IMG-736 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-740 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-743 (human, spondyloepiphyseal dysplasia, congenital) - MWCMG
IMG-747 (human, osteogenesis imperfecta) - MWCMG
IMG-758 (human, Klinefelter syndrome) - MWCMG
IMG-759 (human, Klinefelter syndrome) - MWCMG
IMG-761 (human, thalassemia) - MWCMG
IMG-763 (human, Klinefelter syndrome, mosaic) - MWCMG
IMG-765 (human, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-766 (human, Klinefelter syndrome) - MWCMG
IMG-767 (human, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-768 (human, Klinefelter syndrome, mosaic) - MWCMG
IMG-769 (human, Turner syndrome, mosaic) - MWCMG
IMG-771 (human, Klinefelter syndrome) - MWCMG
IMG-773 (human, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-774 (human, Klinefelter syndrome) - MWCMG
IMG-775 (human, Klinefelter syndrome, mosaic) - MWCMG
IMG-776 (human, Klinefelter syndrome) - MWCMG
IMG-778 (human, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-780 (human, thalassemia) - MWCMG
IMG-785 (human, thalassemia) - MWCMG
IMG-787 (human, thalassemia) - MWCMG
IMG-788 (human, thalassemia) - MWCMG
IMG-796 (human, Edwards' syndrome / trisomy 18) - MWCMG
IMG-797 (human, Edwards' syndrome / trisomy 18) - MWCMG
IMG-807 (human, thalassemia) - MWCMG
IMG-809 (human, thalassemia) - MWCMG
IMG-810 (human, thalassemia) - MWCMG
IMG-811 (human, thalassemia) - MWCMG
IMG-817 (human, X chromosome anomaly) - MWCMG
IMG-819 (human, mucopolysaccharidosis type III B) - MWCMG
IMG-819 XP8CA (human, xeroderma pigmentosum) - MWCMG
IMG-823 (human, Tay-Sachs disease) - MWCMG
IMG-824 (human, Lesch-Nyhan syndrome) - MWCMG
IMG-826 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-827 (human, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-831 (human, X chromosome anomaly) - MWCMG
IMG-847 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-856 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-857 (human, trisomy 22) - MWCMG
IMG-858 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-884 (human, metachromatic leukodystrophy) - MWCMG
IMG-895 (human, Tay-Sachs disease) - MWCMG
IMG-905 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-906 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-907 (human, Tay-Sachs disease) - MWCMG
IMG-908 (human, mucopolysaccharidosis type IV B / Morquio syndrome) - MWCMG
IMG-909 (human, mucopolysaccharidosis type IV B / Morquio syndrome) - MWCMG
IMG-911 (human, mucopolysaccharidosis type IV B / Morquio syndrome) - MWCMG
IMG-915 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-920 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-921 (human, mucopolysaccharidosis type II) - MWCMG
IMG-925 (human, gangliosidosis, generalized GM1, type I) - MWCMG
IMG-926 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-933 (human, mucopolysaccharidosis type IV B / Morquio syndrome) - MWCMG
IMG-934 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-935 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-936 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-938 (human, progeria syndrome) - MWCMG
IMG-939 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-940 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-941 (human, mucopolysaccharidosis type III A) - MWCMG
IMG-944 (human, trisomy 21 / Down syndrome) - MWCMG
IMG-946 (human, trisomy 21 / Down syndrome) - MWCMG
IMG-947 (human, trisomy 21 / Down syndrome) - MWCMG
IMG-948 (human, trisomy 21 / Down syndrome) - MWCMG
IMG-949 (human, Patau syndrome / trisomy 13) - MWCMG
IMG-962 (human, Ehlers-Danlos syndrome) - MWCMG
IMG-963 (human, mucopolysaccharidosis type II) - MWCMG
IMG-964 (human, Gaucher disease) - MWCMG
IMG-965 (human, metachromatic leukodystrophy) - MWCMG
IMG-966 (human, metachromatic leukodystrophy) - MWCMG
IMG-968 (human, mucopolysaccharidosis type II) - MWCMG
IMG-969 (human, mucopolysaccharidosis type II) - MWCMG
IMG-971 (human, mucopolysaccharidosis type II) - MWCMG
IMG-972 (human, mucopolysaccharidosis type II) - MWCMG
IMG-973 (human, mucopolysaccharidosis type II) - MWCMG
IMG-978 (human, poly-X syndrome) - MWCMG
IMG-982 (human, mucopolysaccharidosis type II) - MWCMG
IMG-983 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-984 (human, mucopolysaccharidosis type II) - MWCMG
IMG-985 (human, metachromatic leukodystrophy) - MWCMG
IMG-988 (human, Krabbe disease) - MWCMG
IMG-989 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-990 XP3Br2 (human, xeroderma pigmentosum) - MWCMG
IMG-991 XP3ORO (human, xeroderma pigmentosum) - MWCMG
IMG-994 (human, metachromatic leukodystrophy) - MWCMG
IMG-995 (human, mucopolysaccharidosis type III B) - MWCMG
IMG-996 (human, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-997 (human, Kartagener syndrome X) - MWCMG
IMG-998 (human, Niemann-Pick disease) - MWCMG
IMG-999 (human, gangliosidosis, generalized GM1, type I) - MWCMG
Indian Muntjac (muntjac) - ECACC
Indian Muntjac (muntjac) - GEICH
Indian Muntjac (muntjac) - MWIIW
Indian Muntjac (muntjac) - SPBIC
IP1PV (human, Caucasian, incontinentia pigmenti) - PVCGU
IP2PV (human, Caucasian) - PVCGU
Ja Bos (human, Caucasian, Ehlers-Danlos syndrome) - BGEBS
Jay Sen (human, Caucasian, Ehlers-Danlos syndrome, type I) - BGEBS
LM 1 (human, Caucasian) - BGEBS
LM 10 (human, Caucasian) - BGEBS
LM 11 (human, Caucasian, epidermolysis bullo'sa dystrophica, recessive) - BGEBS
LM 12 (human, Caucasian) - BGEBS
LM 13 (human, Caucasian) - BGEBS
LM 2 (human, Caucasian, Ehlers-Danlos syndrome) - BGEBS
LM 3 (human, Caucasian, Ehlers-Danlos syndrome) - BGEBS
LM 4 (human, Caucasian) - BGEBS
LM 5 (human, Caucasian) - BGEBS
LM 6 (human, Caucasian) - BGEBS
LM 7 (human, Caucasian) - BGEBS
LM 8 (human, Caucasian, Ehlers-Danlos syndrome) - BGEBS
LM 9 (human, Caucasian, Ehlers-Danlos syndrome) - BGEBS
MR (human, Caucasian) - MIUFC
Or De (human, Caucasian, Ehlers-Danlos syndrome, type III) - BGEBS
PVBC-CL247 (human, cutis laxa) - PVUTC
PVBC-CL248 (human, cutis laxa) - PVUTC
PVBC-EDS120 (human, Ehlers-Danlos syndrome, type IV, autosomal dominant) - PVUTC
PVBC-EDS147 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS148 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS149 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS150 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS155 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS170 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS188 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS203 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS211 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS213 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS220 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS223 (human, Ehlers-Danlos syndrome, type VI) - PVUTC
PVBC-EDS27 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS285 (human, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS487 (human, Ehlers-Danlos syndrome, type III) - PVUTC
PVBC-EDS528 (human, Ehlers-Danlos syndrome, type IV, autosomal dominant) - PVUTC
PVBC-EDS546 (human, Ehlers-Danlos syndrome, type IV, autosomal dominant) - PVUTC
PVBC-EDS547 (human, Ehlers-Danlos syndrome, type IV, autosomal dominant) - PVUTC
PVBC-EDS550 (human, Ehlers-Danlos syndrome, type III) - PVUTC
PVBC-I385 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-MF115 (human, Marfan syndrome) - PVUTC
PVBC-MF255 (human, Marfan syndrome) - PVUTC
PVBC-MF256 (human, Marfan syndrome) - PVUTC
PVBC-MF257 (human, Marfan syndrome) - PVUTC
PVBC-MF267 (human, Marfan syndrome) - PVUTC
PVBC-MF268 (human, Marfan syndrome) - PVUTC
PVBC-MF269 (human, Marfan syndrome) - PVUTC
PVBC-MF270 (human, Marfan syndrome) - PVUTC
PVBC-MF354 (human, Marfan syndrome) - PVUTC
PVBC-MF375 (human, Marfan syndrome) - PVUTC
PVBC-MF376 (human, Marfan syndrome) - PVUTC
PVBC-MF377 (human, Marfan syndrome) - PVUTC
PVBC-MF422 (human, Marfan syndrome) - PVUTC
PVBC-MF423 (human, Marfan syndrome) - PVUTC
PVBC-MF424 (human, Marfan syndrome) - PVUTC
PVBC-MF448 (human, Marfan syndrome) - PVUTC
PVBC-MF538 (human, Marfan syndrome) - PVUTC
PVBC-OI (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI108 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI121 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI127 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI129 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI133 (human, osteogenesis imperfecta, atypical) - PVUTC
PVBC-OI157 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI158 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI159 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI160 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI161 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI164 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI165 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI172 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI184 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI185 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI186 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI187 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI189 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI193 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI197 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI204 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI205 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI206 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI217 (human, osteogenesis imperfecta) - PVUTC
PVBC-OI227 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI228 (human, osteogenesis imperfecta) - PVUTC
PVBC-OI230 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI234 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI250 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI254 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI265 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI271 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI272 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI273 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI274 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI275 (human, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI276 (human, osteogenesis imperfecta, type I/EDS, atypical) - PVUTC
PVBC-OI277 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI284 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI291 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI299 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI305 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI306 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI307 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI313 (human, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI314 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI317 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI325 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI330 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI332 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI340 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI347 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI348 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI350 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI356 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI370 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI371 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI373 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI378 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI379 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI380 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI383 (human, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI384 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI387 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI388 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI396 (human) - PVUTC
PVBC-OI427 (human) - PVUTC
PVBC-OI428 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI433 (human) - PVUTC
PVBC-OI437 (human) - PVUTC
PVBC-OI440 (human, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI443 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI444 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI449 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI452 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI453 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI460 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI461 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI462 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI464 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI465 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI466 (human, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI467 (human, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI471 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI488 (human) - PVUTC
PVBC-OI489 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI499 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI500 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI522 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI531 (human, osteogenesis imperfecta, type I/EDS, atypical) - PVUTC
PVBC-OI535 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI540 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI55 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI553 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI555 (human, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI559 (human, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI65 (human, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI82 (human, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-Pr110 (human, prolidase deficiency) - PVUTC
PVBC-Pr152 (human, prolidase deficiency) - PVUTC
PVBC-Pr260 (human, prolidase deficiency) - PVUTC
PVBC-Pr98 (human, prolidase deficiency) - PVUTC
PVCB-EDS516 (human, Ehlers-Danlos syndrome, type IV, autosomal dominant) - PVUTC
RAB-9 (rabbit, New Zealand white) - ECACC
RAB-9 (rabbit, New Zealand white) - IZSBS
RRAm1 (rat) - ICLC
RS-537 (rabbit) - MWIIW
SC (human, Marfan syndrome) - BGEBS
TTD10PV (human, Caucasian, trichotiodystrophy + xeroderma pigmentosum) - PVCGU
TTD11PV (human, Caucasian, trichotiodystrophy + xeroderma pigmentosum) - PVCGU
TTD1PV (human, Caucasian, trichotiodystrophy + xeroderma pigmentosum) - PVCGU
TTD2PV (human, Caucasian, trichotiodystrophy + xeroderma pigmentosum) - PVCGU
TTD3PV (human, Caucasian, trichotiodystrophy + xeroderma pigmentosum) - PVCGU
TTD4PV (human, Caucasian, trichotiodystrophy + xeroderma pigmentosum) - PVCGU
TTD5PV (human, Caucasian, hair - brain syndrome) - PVCGU
TTD6PV (human, Caucasian, trichotiodystrophy + xeroderma pigmentosum) - PVCGU
TTD7PV (human, Caucasian, trichotiodystrophy + xeroderma pigmentosum) - PVCGU
TTD8PV (human, Caucasian, trichotiodystrophy + xeroderma pigmentosum) - PVCGU
TTD9PV (human, Caucasian, hair - brain syndrome) - PVCGU
TTDH10PV (human, Caucasian) - PVCGU
TTDH11PV (human, Caucasian) - PVCGU
TTDH12PV (human, Caucasian) - PVCGU
TTDH1PV (human, Caucasian) - PVCGU
TTDH2PV (human, Caucasian) - PVCGU
TTDH3PV (human, Caucasian) - PVCGU
TTDH4PV (human, Caucasian) - PVCGU
TTDH5PV (human, Caucasian) - PVCGU
TTDH6PV (human, Caucasian) - PVCGU
TTDH7PV (human, Caucasian) - PVCGU
TTDH8PV (human, Caucasian) - PVCGU
TTDH9PV (human, Caucasian) - PVCGU
VP-8 (human, pyroglutamicaciduria / 5-oxoprolinuria) - RMSTC
VS86 (human, trisomy 21 / Down syndrome) - GGB
XP10PV (human, Caucasian, xeroderma pigmentosum III) - PVCGU
XP11PV (human, Caucasian, xeroderma pigmentosum I) - PVCGU
XP12PV (human, Caucasian, xeroderma pigmentosum III) - PVCGU
XP13PV (human, Caucasian, xeroderma pigmentosum III) - PVCGU
XP14PV (human, Caucasian, xeroderma pigmentosum with normal DNA repair rates) - PVCGU
XP15PV (human, Caucasian, xeroderma pigmentosum IV) - PVCGU
XP16PV (human, Caucasian, xeroderma pigmentosum IV) - PVCGU
XP17PV (human, Caucasian, xeroderma pigmentosum IV) - PVCGU
XP18PV (human, Caucasian, xeroderma pigmentosum III) - PVCGU
XP19PV (human, Caucasian, xeroderma pigmentosum III) - PVCGU
XP21PV (human, Caucasian, xeroderma pigmentosum) - PVCGU
XP22PV (human, Caucasian, xeroderma pigmentosum) - PVCGU
XP23PV (human, Caucasian, xeroderma pigmentosum) - PVCGU
XP24PV (human, Caucasian, xeroderma pigmentosum) - PVCGU
XP5PV (human, Caucasian, xeroderma pigmentosum III) - PVCGU
XP9PV (human, Caucasian, xeroderma pigmentosum III) - PVCGU
XPH10PV (human, Caucasian) - PVCGU
XPH11PV (human, Caucasian) - PVCGU
XPH12PV (human, Caucasian) - PVCGU
XPH13PV (human, Caucasian) - PVCGU
XPH14PV (human, Caucasian) - PVCGU
XPH15PV (human, Caucasian) - PVCGU
XPH16PV (human, Caucasian) - PVCGU
XPH17PV (human, Caucasian) - PVCGU
XPH18PV (human, Caucasian) - PVCGU
XPH19PV (human, Caucasian) - PVCGU
XPH1PV (human, Caucasian) - PVCGU
XPH20PV (human, Caucasian) - PVCGU
XPH2PV (human, Caucasian) - PVCGU
XPH3PV (human, Caucasian) - PVCGU
XPH4PV (human, Caucasian) - PVCGU
XPH5PV (human, Caucasian) - PVCGU
XPH6PV (human, Caucasian) - PVCGU
XPH7PV (human, Caucasian) - PVCGU
XPH8PV (human, Caucasian) - PVCGU
XPH9PV (human, Caucasian) - PVCGU
XTK1 (hamster, Syrian) - MWIIW
XTK2 (hamster, Syrian) - MWIIW


For information, get in touch with:
IRCCS Ospedale Policlinico San Martino
Largo Rosanna Benzi, 10 - I-16132 Genova - Italy
Dott.ssa Barbara Parodi
Email: barbara.parodi@hsanmartino.it

If you want to cite CLDB and HyperCLDB, please use the following reference:

P. Romano, A. Manniello, O. Aresu, M. Armento, M. Cesaro, B. Parodi.
Cell Line Data Base: structure and recent improvements towards molecular authentication of human cell lines.
Nucleic Acids Research 2009 37(Database issue):D925-D932.
DOI: doi:10.1093/nar/gkn730; PMID: 18927105