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Summary Literature (0)
MIM:307700 - HYPOPARATHYROIDISM, X-LINKED; HYPX

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010618 - familial isolated hypoparathyroidism due to agenesis of parathyroid gland
MONDO:0016390 - familial hypoparathyroidism

Disease Ontology (DO):
DOID:11199 - hypoparathyroidism