autosomal dominant hypocalcemia 2

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Summary

Literature (0)

DOID:0090108 - autosomal dominant hypocalcemia 2

Disease Ontology Definition:An autosomal dominant hypocalcemia that has_material_basis_in heterozygous mutation in the G protein subunit alpha 11 gene (GNA11) on chromosome 19p13.

Synonyms: HYPOC2

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

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014146 - autosomal dominant hypocalcemia 2

MONDO:0014146 - autosomal dominant hypocalcemia 2

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

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

Parent(s): autosomal dominant hypocalcemia (is_a)