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DO Term : holoprosencephaly 2 [DOID:0110872] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A holoprosencephaly that has_material_basis_in mutation in the homeobox-containing SIX3 gene on chromosome 2p21.

synonyms:
MESH:C563579,
OMIM:157170,
157170,
HPE2

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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