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Summary Literature (0)
MIM:146200 - HYPOPARATHYROIDISM, FAMILIAL ISOLATED, 1; FIH1

Xenbase Genes: gcm2, pth, casr

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007796 - hypoparathyroidism, familial isolated 1
MONDO:0016000 - familial isolated hypoparathyroidism due to impaired PTH secretion
MONDO:0016390 - familial hypoparathyroidism

Disease Ontology (DO):
DOID:0111387 - familial isolated hypoparathyroidism
DOID:11199 - hypoparathyroidism