OBO ID: DOID:0111441
Term Name: optic atrophy 1 Search Ontology:
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:
OTHER optic atrophy 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
OPA1 Optic atrophy 1 165500
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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