hereditary optic atrophy
MONDO:0043878Mondo
Findings
No curated finding names hereditary optic atrophy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A family of inherited disorders characterized by progressive loss of vision secondary to death of the retinal ganglion cell axons that comprise the optic nerve.
Definition from the Mondo Disease Ontology (MONDO:0043878), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (15)
- ACO2-related optic atrophy with or without extraocular features
- autosomal dominant optic atrophy
- autosomal recessive optic atrophy, OPA7 type
- Leber hereditary optic neuropathy
- optic atrophy 10 with or without ataxia, intellectual disability, and seizures
- optic atrophy 11
- optic atrophy 12
- optic atrophy 13 with retinal and foveal abnormalities
- optic atrophy 14
- optic atrophy 15
- optic atrophy 16
- optic atrophy 2
- optic atrophy 4
- optic atrophy 6
- osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome