Search Ontology:
Human Disease
optic atrophy 5
- Term ID
- DOID:0111438
- Synonyms
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- OPA5
- Definition
- An optic atrophy characterized by degeneration of retinal ganglion cells resulting in slowly progressive visual loss with variable onset from the first to third decades that has_material_basis_in heterozygous of mutation in DNM1L on chromosome 12p11.21. https://www.ncbi.nlm.nih.gov/pubmed/28969390
- References
- Ontology
- Human Disease ( DOID:0111438 )
- is a type of
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Genes Involved
Zebrafish Models