rhegmatogenous retinal detachment, autosomal dominant

Preferred Label : rhegmatogenous retinal detachment, autosomal dominant;

MeSH synonym : DRRD;

Origin ID

C563710;

UMLS CUI

C1836081;

Automatic exact mappings (from CISMeF team)
- Stickler syndrome, type I, nonsyndromic ocular [OMIM Phenotype]
Currated CISMeF NLP mapping
- Autosomal dominant rhegmatogenous retinal detachment [ICD-11 More detail]
- Autosomal dominant rhegmatogenous retinal detachment [ORDO Disease]
- Autosomal dominant rhegmatogenous retinal detachment (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- eye diseases, hereditary [MeSH Descriptor]
- retinal detachment [MeSH Descriptor]
Record concept(s)
- rhegmatogenous retinal detachment, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant rhegmatogenous retinal detachment [ORDO Disease]
- Autosomal dominant rhegmatogenous retinal detachment (disorder) [SNOMED CT concept]