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
06885 AMD dysplasia, acromesomelic - - 2 2 BMPR1B, GDF5, NPR2, PRKG2 - -
06883 AMD4 dysplasia, acromesomelic, type 4 619636 - - - PRKG2 - -
06884 SMDP dysplasia, spondylometaphyseal, Pagnamenta type 619638 - - - PRKG2 - -
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