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Summary Literature (0)
MIM:605635 - HYPERALDOSTERONISM, FAMILIAL, TYPE II; HALD2

Xenbase Genes: clcn2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011576 - familial hyperaldosteronism type II

Disease Ontology (DO):
DOID:446 - primary hyperaldosteronism