Autosomal-Dominant optic atrophy

Preferred Label : Autosomal-Dominant optic atrophy;

ICD-11 definition : Optic nerve disorders inherited in an autosomal dominant manner;

ICD-11 synonym : Dominant optic atrophy;

Détails

Origin ID

524458469;

Automatic exact mappings (from CISMeF team)
- Autosomal Dominant Optic Atrophy [NCIt concept]
- Autosomal dominant optic atrophy [ORDO Disease]
- Dominant hereditary optic atrophy (disorder) [SNOMED CT concept]
- Hagemoser Weinstein Bresnick syndrome [MeSH concept]
- optic atrophy, autosomal dominant [MeSH Descriptor]
- optic atrophy, autosomal dominant [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients