All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02163 ODG2;POF4 dysgenesis, ovarian, type 2 (premature ovarian failure, type 4) 300510 XL - - BMP15 - -
05296 OI osteogenesis imperfecta - - 4591 1414 BMP1, CCDC134, COL1A1, COL1A2, CREB3L1, CRTAP, FAM46A, FKBP10, IFITM5, KDELR2, KIF5B, MBTPS2, MESDC2, P3H1, PHLDB1, SERPINF1, SERPINH1, SP7, SPARC, TMEM38B, WNT1 - -
03752 OI13 osteogenesis imperfecta, type XIII (OI13) 614856 AR 3 3 BMP1 - -
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