All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00250 - rickets, hypophosphatemic, X-linked recessive 300554 - 2 2 CLCN5 - -
00252 - proteinuria, hypercalciuria, nephrocalcinosis 308990 - 4 4 CLCN5 - -
00249 DENT-1 Dent disease, type 1 300009 - 223 215 CLCN5 - -
04154 NPHL-2 nephrolithiasis, type 2 (NPHL-2) - - 0 0 CLCN5 - -
00251 XRN-1 nephrolithiasis, X-linked, with renal failure, type 1 (XRN-1) 310468 - 8 8 CLCN5 - -
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