Related Conditions
Autosomal dominant optic atrophy plus syndrome(child)
Autosomal dominant optic atrophy classic form(child)
Autosomal dominant optic atrophy and peripheral neuropathy syndrome(child)
Autosomal dominant optic atrophy and cataract(child)
Bosch Boonstra Schaaf optic atrophy syndrome(child)
Autosomal dominant hereditary disorder(parent)
Hereditary optic atrophy(parent)
Quick Facts
- SNOMED CT
- 2065009
- UMLS CUI
- C4551508
- Fully Specified Name
- Dominant 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.