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Summary Literature (1)
OMIM:613677 - HYPERALDOSTERONISM, FAMILIAL, TYPE III; HALD3


Xenbase Genes: kcnj5

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013359 - familial hyperaldosteronism type III

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