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DO Term : holoprosencephaly 9 [DOID:0110873] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14.

synonyms:
holoprosencephaly with microphthalmia and first branchial arch anomalies,
OMIM:610829,
610829,
MESH:C563659,
HPE9,
pituitary anomalies with holoprosencephaly-like features

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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