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DO Term : anterior segment dysgenesis 2 [DOID:0080607] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An anterior segment dysgenesis that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the FOXE3 gene on chromosome 1p33.

synonyms:
OMIM:610256,
610256

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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