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DO Term : familial isolated hypoparathyroidism [DOID:0111387] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
OMIM:146200,
146200,
FIH

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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