telangiectasia, generalized essential

Preferred Label : telangiectasia, generalized essential;

Origin ID

C562998;

UMLS CUI

C0473555;

Automatic exact mappings (from CISMeF team)
- Generalised essential telangiectasia [ICD-11 Subcategory]
- Telangiectasia, hereditary benign [OMIM Phenotype]
Currated CISMeF NLP mapping
- Generalized essential telangiectasia [ORDO Disease]
- Generalized essential telangiectasia (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- telangiectasis [MeSH Descriptor]
Record concept(s)
- telangiectasia, generalized essential [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Generalized essential telangiectasia [ORDO Disease]
- Generalized essential telangiectasia (disorder) [SNOMED CT concept]