Overview
Hereditary optic atrophy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Hereditary sensory and motor neuropathy, type VI(child)
Dominant hereditary optic atrophy(child)
Leber's optic atrophy(child)
Hereditary right optic atrophy(child)
Hereditary left optic atrophy(child)
Wolfram-like syndrome(child)
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome(child)
Infantile cerebellar and retinal degeneration(child)
Autosomal recessive optic atrophy OPA7 type(child)
Lethal ataxia-deafness-optic atrophy(child)
SPOAN and SPOAN-related disorder(child)
Autosomal recessive optic atrophy type 6(child)
Childhood-onset autosomal dominant optic atrophy(child)
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome(child)
X-linked optic atrophy(child)
MEPAN syndrome(child)
ANOAC (axonal neuropathy, optic atrophy, cognitive deficit) syndrome(child)
Primary optic atrophy(parent)
Inherited optic neuropathy(parent)
Hereditary degenerative disease of central nervous system(parent)
Quick Facts
- SNOMED CT
- 26360005
- UMLS CUI
- C0029125
- Fully Specified Name
- Hereditary optic atrophy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.