Disease association ontology term - MONDO:0008134 - autosomal dominant optic atrophy, classic form
Term summary
- ID
- MONDO:0008134
- Name
- autosomal dominant optic atrophy, classic form
- Ontology or CV name
- Disease association
- Definition
- One of the most common forms of hereditary optic neuropathy characterized by progressive bilateral visual loss during the first decade of life, associated with optic disk pallor, visual field and color vision defects.
