All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00252 - proteinuria, hypercalciuria, nephrocalcinosis 308990 XLR 20 20 CLCN5 - -
00249 DENT1 Dent disease, type 1 300009 XLR 252 245 CLCN5 - -
06886 hypophosphatemia hypophosphatemia - - 1467 1447 CLCN5, FGF23, PHEX - -
04154 NPHL nephrolithiasis - - 1 1 CLCN5, SLC26A6, SLC9A3R1 - -
00250 XLHRR rickets, hypophosphatemic, X-linked recessive 300554 XLR 2 2 CLCN5 - -
00251 XRN nephrolithiasis, Xlinked, with renal failure, type 1 (XRN1) 310468 XLR 8 8 CLCN5 - -
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