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 hypophosphatemia hypophosphatemia - - 1467 1447 CLCN5, FGF23, PHEX - -
02241 XLHRD rickets, hypophosphatemic, X-linked dominant 307800 XLD 940 904 PHEX - -
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