All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06886 HR hypophosphataemic rickets - - 672 651 CLCN5, FGF23, PHEX - -
02241 XLHR rickets, hypophosphatemic, X-linked dominant (XLHR) 307800 XLD 939 903 PHEX - -
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