All diseases

OMIM ID
145260
OMIM term:
PSEUDOHYPOALDOSTERONISM, TYPE IIA; PHA2A
Alternative terms:
HYPERPOTASSEMIA AND HYPERTENSION, FAMILIAL
HYPERTENSIVE HYPERKALEMIA, FAMILIAL
GORDON HYPERKALEMIA-HYPERTENSION SYNDROME
(∗) Location:
1q31-q42  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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