poikiloderma, hereditary sclerosing

Preferred Label : poikiloderma, hereditary sclerosing;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0563124;

UMLS CUI

C0343094;

Automatic exact mappings (from CISMeF team)
- Hereditary sclerosing poikiloderma [ICD-11 More detail]
Currated CISMeF NLP mapping
- Hereditary sclerosing poikiloderma (disorder) [SNOMED CT concept]
- Poikiloderma, hereditary sclerosing [OMIM Phenotype]
Related record
- poikiloderma, hereditary sclerosing [MeSH Supplementary Concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary sclerosing poikiloderma (disorder) [SNOMED CT concept]
- Poikiloderma, hereditary sclerosing [OMIM Phenotype]