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DO Term : autosomal dominant hypocalcemia [DOID:0090109] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
ORDO:428,
PS601198,
HYPOC,
ICD10CM:E20.8,
OMIM:PS601198,
GARD:2877

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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