| Term Name: | optic atrophy 12 |
|---|---|
| Synonyms: | |
| 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. |
| Ontology: | Human Disease [DOID:0080840] ( DOID:0080840 ) |