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Summary Literature (0)
MIM:601198 - HYPOCALCEMIA, AUTOSOMAL DOMINANT 1; HYPOC1

Xenbase Genes: casr

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011013 - autosomal dominant hypocalcemia 1
MONDO:0015231 - Bartter syndrome
MONDO:0016390 - familial hypoparathyroidism
MONDO:0016983 - Bartter syndrome with hypocalcemia