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DOID:0090108 - autosomal dominant hypocalcemia 2
Disease Ontology Definition:An autosomal dominant hypocalcemia disease that has material_basis_in heterozygous mutation in the GNA11 gene on chromosome 19p13.
Synonyms: HYPOC2,
Xenbase Genes : gna11
MONDO:0014146 - autosomal dominant hypocalcemia 2 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant hypocalcemia (is_a)