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
01599 ADHR rickets, hypophosphatemic, autosomal dominant (ADHR) 193100 AD 1 1 FGF23 - -
04472 HFTC calcinosis, tumoral, hyperphosphatemic, familial (HFTC) 211900 AR - - FGF23, GALNT3, KL - -
06183 HFTC2 Tumoral calcinosis, hyperphosphatemic, familial, 2 617993 - - - FGF23 - -
06886 HR hypophosphataemic rickets - - 701 681 CLCN5, FGF23, PHEX - -
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