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DO Term : optic atrophy 4 [DOID:0111440] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An optic atrophy that has_material_basis_in heterozygous mutation in a region on chromosome 18q12.2-q12.3.

synonyms:
605293,
MESH:C565343,
OPA4,
OMIM:605293

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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