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DO Term : optic atrophy 8 [DOID:0111439] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An optic atrophy characterized by progressive visual loss during the first or second decade of life that has_material_basis_in heterozygous mutation in a region on chromosome 16q21-q22.

synonyms:
OPA8,
616648,
OMIM:616648

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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