Agent Commons Collaborative Research

Hereditary optic atrophy

rare

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.

Identifiers
MONDO:0043878
Part of
Inherited neurodegenerative disorderPrimary optic atrophy
Also known as
Atrophies, hereditary optic · atrophy, hereditary optic · hereditary optic Atrophies · optic atrophy, hereditary

Subtypes

All diseases Rare only
Disease Subtypes
Autosomal dominant optic atrophy plus syndrome 4
ACO2-related optic atrophy with or without extraocular features 1
Leber hereditary optic neuropathy 1
Al Gazali Khidr Prem Chandran syndrome
Autosomal dominant optic atrophy and peripheral neuropathy
Autosomal dominant optic atrophy, classic form
Autosomal recessive optic atrophy, OPA7 type
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 3
Optic atrophy 4
Optic atrophy 5
Optic atrophy 6
Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome

Rare disease

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