autosomal dominant optic atrophy
MONDO:0020250Mondo
Findings
No curated finding names autosomal dominant optic atrophy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss.
Definition from the Mondo Disease Ontology (MONDO:0020250), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- SPG7HGNC:11237
- Strong · PanelApp Australia · Autosomal dominant · 2025
Where it sits
Other names
3 names
Resolves to: autosomal dominant optic atrophy
- Also called
- ADOADOAoptic atrophy, autosomal dominant