Search Ontology:
Human Disease

optic atrophy 1

Term ID
DOID:0111441
Synonyms
  • OPA1
Definition
An optic atrophy characterized by early childhood onset of visual impairment, temporal optic disc pallor, color vision deficits, and centrocecal scotoma of variable density that has_material_basis_in heterozygous mutation in the OPA1 gene on chromosome 3q29. (3)
References
Ontology
Human Disease   ( DOID:0111441 )
Relationships
is a type of
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Genes Involved
Zebrafish Models