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
04154 NPHL nephrolithiasis - - 1 1 CLCN5, SLC26A6, SLC9A3R1 - -
03114 NPHLOP2 nephrolithiasis/osteoporosis, hypophosphatemic, type 2 (NPHLOP-2) 612287 AD - - SLC9A3R1 - -
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