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DOID:0090109 - autosomal dominant hypocalcemia
Disease Ontology Definition:A calcium metabolism disease characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone.
Synonyms: HYPOC,
Echinobase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
calcium metabolism disease (is_a)