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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

Controlled terms of pathologies

Names beginning by O

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
omphalocele 164750 164750 1
ornithine-transcarbamylase deficiency *311250 311250 1
osteogenesis imperfecta #166210 166210 20
osteogenesis imperfecta type I (with opalescent teeth) 166240 166240 17
osteogenesis imperfecta, atypical OMIM Home 1
osteogenesis imperfecta, type I (with blue sclerae) #166200 166200 49
osteogenesis imperfecta, type I neurofibr. #166200 166200 1
osteogenesis imperfecta, type I/EDS, atypical OMIM Home 2
osteogenesis imperfecta, type II #166210 166210 17
osteogenesis imperfecta, type III with normal sclerae #259420 259420 31
osteogenesis imperfecta, type IV #166220 166220 18
osteopetrosis autosomal recessive #259700 259700 1
osteoporosis-pseudoglioma syndrome *259770 259770 2

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