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

Controlled terms of pathologies

Names beginning by M

OMIM(TM), Online Mendelian Inheritance in Man, is a catalog of human genes and genetic disorders authored and edited by Dr. Victor A. McKusick and colleagues at Johns Hopkins and elsewhere. The database contains textual information, pictures, and reference information.

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Pathology nameLink to OMIMNo. of cells
malformations OMIM Home 1
mannosidosis, alpha b, lysosomal *248500 248500 10
maple syrup urine disease *248600 248600 7
Marek's disease OMIM Home 1
Marfan syndrome #154700 154700 34
Marinesco-Sjogren syndrome *248800 248800 1
Martin-Bell syndrome *309550 309550 5
McCune-Albright sindrome #174800 174800 1
Meckel syndrome *249000 249000 1
Melnick-Needles syndrome 249420 249420 1
Menkes syndrome #309400 309400 7
metachromatic leukodystrophy #249900 249900 10
metachromatic leukodystrophy, late-infantile *250100 250100 32
metatropic dwarfism, type II #156550 156550 2
methylenetetra-hydrofolate reductase def. OMIM Home 2
methylmalonicacidemia *251000 251000 12
Miller-Dieker syndrome #247200 247200 2
mitochondrial respiratory chain complex I #252010 252010 1
molybdenum cofactor deficiency #252150 252150 1
mucolipidosis OMIM Home 1
mucolipidosis II *252500 252500 30
mucolipidosis III *252600 252600 5
mucopolysaccharidosis type I / Hurler disease *252800 252800 51
mucopolysaccharidosis type II *309900 309900 67
mucopolysaccharidosis type III A *252900 252900 35
mucopolysaccharidosis type III B *252920 252920 20
mucopolysaccharidosis type III C *252930 252930 9
mucopolysaccharidosis type III D *252940 252940 3
mucopolysaccharidosis type IV A *253000 253000 19
mucopolysaccharidosis type IV B / Morquio syndrome *253010 253010 7
mucopolysaccharidosis type VI *253200 253200 7
multiple carboxylase deficiency, biotin-responsive *253270 253270 1
multiple carboxylase deficiency, late-onset *253260 253260 1
multiple malformations OMIM Home 1
muscolar dystrophy def.sarcoglican *253700 253700 1
myopathy with deficiency of CPT I 255120 255120 1


For information, get in touch with:
IRCCS AOU San Martino IST,
c/o Centro Biotecnologie Avanzate, Torre D - Piano 2

Largo Rosanna Benzi, 10 - I-16132 Genova - Italy
Dott.ssa Assunta Manniello
Email: mariaassunta.manniello@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