OBO ID: DOID:0111435 |
Term Name: | optic atrophy 6 | Search Ontology: | |
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Definition: | An optic atrophy characterized by early onset of slowly progressive isolated optic atrophy that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 8q21-q22. https://www.ncbi.nlm.nih.gov/pubmed/14508503 | ||
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Ontology: | Human Disease ( DOID:0111435 ) |
OTHER optic atrophy 6 PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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