Agent Commons Collaborative Research
Optic atrophy 2
rareA rare form of hereditary optic atrophy, seen in only 4 families to date, with an onset in early childhood, characterized by progressive loss of visual acuity, significant optic nerve pallor and occasionally additional neurological manifestations, with females being unaffected.
- Identifiers
- MONDO:0010698 OMIM:311050Orphanet:98890
- Part of
- Hereditary optic atrophy
- Also known as
- non-Leber type optic atrophy with early-onset · OPA2 · optic atrophy 2, X-linked · optic atrophy type 2
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