All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06885 AMD dysplasia, acromesomelic - - 2 2 BMPR1B, GDF5, NPR2, PRKG2 - -
00185 AMD3 dysplasia, acromesomelic, type 3, Demirhan 609441 AR - - BMPR1B - -
06618 BDA1D Brachydactyly, type A1, D 616849 AD - - BMPR1B - -
00184 BDA2 brachydactyly, type A2 (BD-A2) 112600 AD - - BMP2, BMPR1B, GDF5 - -
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