All diseases

OMIM ID
263800
OMIM term:
GITELMAN SYNDROME
Alternative terms:
HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
POTASSIUM AND MAGNESIUM DEPLETION
(∗) Location:
16q13  
(†) Associated OMIM genes:
SLC12A3  
(‡) Associated MGI genes:
Slc12a3   Stk39   Wnk4  

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