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DO Term : combined pituitary hormone deficiency 6 [DOID:0061022] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A combined pituitary hormone deficiency that has_material_basis_in heterozygous mutation in the OTX2 gene on chromosome 14q21.

synonyms:
613986,
OMIM:613986,
CPHD6

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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