OBO ID: DOID:0080840 |
Term Name: | optic atrophy 12 | Search Ontology: | |
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Definition: | An optic atrophy that is characterized by slowly progressive visual impairment with onset usually in the first decade and that has_material_basis_in heterozygous mutation in the AFG3L2 gene on chromosome 18p11. https://pubmed.ncbi.nlm.nih.gov/32219868/ | ||
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Ontology: | Human Disease ( DOID:0080840 ) |
OTHER optic atrophy 12 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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