Phenotypes for disease #00637 (OI2 (osteogenesis imperfecta, type II (OI2)), OMIM:166210)

11 entries on 1 page. Showing entries 1 - 11.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000104265 - - - Familial, autosomal dominant - - - - - Karina Silveira 00132059
0000104266 - - - Familial, autosomal dominant - - - - - Karina Silveira 00132061
0000257286 respiratory support from birth; most radiological and clinical features consistent with type 2 OI (some features more consistent with type 3); died at 11 weeks of age from respiratory failure OI type 2 - Isolated (sporadic) - - - - - Ajay Kevat 00361893
0000325229 - - - Unknown 00m00y - - - - Kim Worring 00434982
0000325247 - - - Unknown 00y00m - - - - Kim Worring 00435007
0000325248 - - - Unknown 00y00m - - - - Kim Worring 00435008
0000325249 - - - Unknown 00y00m - - - - Kim Worring 00435009
0000325250 - - - Unknown 00y00m - - - - Kim Worring 00435010
0000325251 - - - Unknown 00y00m - - - - Kim Worring 00435011
0000325252 - - - Unknown 00y00m - - - - Kim Worring 00435012
0000325259 - - - Unknown 00y00m - - - - Kim Worring 00435017
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