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
00185 ACGA chondrodysplasia, acromesomelic, with genital anomalies (ACGA) 609441 - - - BMPR1B - -
00191 AMDG chondrodysplasia, acromesomelic, type Grebe (AMDG) 200700 - - - BMPR1B, GDF5 - -
00184 BD-A2 brachydactyly, type A2 (BD-A2) 112600 - - - BMP2, BMPR1B, GDF5 - -
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