Childhood-onset autosomal dominant optic atrophy

disorder

SNOMED 838307002CUI C5395054

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary optic atrophy(parent)

Quick Facts

SNOMED CT: 838307002
UMLS CUI: C5395054
Fully Specified Name: Childhood-onset autosomal dominant 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.