autosomal dominant hypocalcemia

Summary

DOID:0090109 - autosomal dominant hypocalcemia

Disease Ontology Definition:A metal metabolism disorder characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone.

Synonyms: HYPOC,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: gna11, casr

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0018543 - autosomal dominant hypocalcemia

MONDO:0018543 - autosomal dominant hypocalcemia

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), calcium metabolism disease (is_a), metal metabolism disorder (is_a)