OBO ID: DOID:0111441 |
Term Name: | optic atrophy 1 | Search Ontology: | |
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Synonyms: |
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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) | ||
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Ontology: | Human Disease ( DOID:0111441 ) |
OTHER optic atrophy 1 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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