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 - -
02442 AMD1 dysplasia, acromesomelic, type 1, Maroteaux 602875 AR 34 33 NPR2 - autosomal recessive
04134 ECDM chondrodysplasia, epiphyseal, Miura type (ECDM) 615923 AD - - NPR2 - -
04597 SNSK stature, short, with nonspecific skeletal abnormalities (SNSK) 616255 AD - - NPR2 - -
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