Zinsser-Cole-Engman syndrome

Preferred Label : Zinsser-Cole-Engman syndrome;

UMLS semantic type : T019 - Congenital Abnormality; T047 - Disease or Syndrome;

Origin ID

M0385213;

UMLS CUI

C1148551;

Automatic exact mappings (from CISMeF team)
- Dyskeratosis congenita, X-linked [OMIM Phenotype]
- X-linked dyskeratosis congenita [DO Concept]
Currated CISMeF NLP mapping
- Congenital dyskeratosis [MedDRA Preferred Term]
- Dyskeratosis Congenita [NCIt concept]
- Dyskeratosis congenita [PASCAL descriptor]
- Dyskeratosis congenita [ICD-11 More detail]
- Dyskeratosis congenita [ORDO Disease]
- Dyskeratosis congenita (disorder) [SNOMED CT concept]
- dyskeratosis congenita [Disease (Nov.)]
- dyskeratosis congenita [DO Concept]
- dyskeratosis congenita [SNOMED Notion]
Related record
- dyskeratosis congenita [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dyskeratosis congenita [PASCAL descriptor]
- Dyskeratosis congenita, X-linked [OMIM Phenotype]
- X-Linked Dyskeratosis Congenita [NCIt concept]
- X-linked dyskeratosis congenita [DO Concept]
- X-linked dyskeratosis congenita (disorder) [SNOMED CT concept]