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Summary Literature (0)
MIM:615361 - HYPOCALCEMIA, AUTOSOMAL DOMINANT 2; HYPOC2

Xenbase Genes: gna11

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014146 - autosomal dominant hypocalcemia 2
MONDO:0016390 - familial hypoparathyroidism
MONDO:0018543 - lumen of intestine