poikiloderma, hereditary sclerosing

Preferred Label : poikiloderma, hereditary sclerosing;

Is substance : O;

Origin ID

C562824;

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]
MeSH term(s) associated for indexing
- sclerosis [MeSH Descriptor]
- skin abnormalities [MeSH Descriptor]
- skin diseases, genetic [MeSH Descriptor]
Record concept(s)
- poikiloderma, hereditary sclerosing [MeSH 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]