All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00910 FRTS2 Fanconi renotubular syndrome, type 2 (FRTS-2) 613388 AR 1 - SLC34A1 - -
05195 HCINF2 hypercalcemia, infantile, type 2 (HCINF-2) 616963 AR 17 17 SLC34A1 - -
00909 NPHLOP1 nephrolithiasis/osteoporosis, hypophosphatemic, type 1 (NPHLOP-1) 612286 AD - - SLC34A1 - -
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