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Echinobase
Summary Literature (0)
DOID:0111387 - familial isolated hypoparathyroidism

Disease Ontology Definition:A hypoparathyroidism that has_material_basis_in mutation in PTH on chromosome 6p24.2 or in the GCM2 gene on chromosome 11p15.3.

Synonyms: FIH,

Echinobase Genes :


OMIM:
MIM:146200 - hypoparathyroidism, familial isolated; fih

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hypoparathyroidism (is_a)