Mydriasis, congenital

Preferred Label : Mydriasis, congenital;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 159420;

Détails

Origin ID

159420;

UMLS CUI

C1303010;

Automatic exact mappings (from CISMeF team)
- Congenital mydriasis [ICD-11 More detail]
Currated CISMeF NLP mapping
- Congenital mydriasis (disorder) [SNOMED CT concept]
- mydriasis, congenital [MeSH concept]
- mydriasis, congenital [MeSH Supplementary Concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital mydriasis (disorder) [SNOMED CT concept]
- mydriasis, congenital [MeSH Supplementary Concept]
- mydriasis, congenital [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