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DO Term : optic atrophy 2 [DOID:0111443] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An optic atrophy that has_material_basis_in variation in a region on chromosome Xp11.4-p11.21.

synonyms:
X-linked optic atrophy 2,
311050,
OPA2,
OMIM:311050

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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