dyskeratosis, hereditary benign intraepithelial - CISMeF

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Dyskeratosis, hereditary benign intraepithelialMeSH Supplementary Concept

Preferred Label : dyskeratosis, hereditary benign intraepithelial;

Details

Origin ID

C562551;

UMLS CUI

C0265966;

Automatic exact mappings (from CISMeF team)
- Hereditary benign intraepithelial dyskeratosis [ORDO Disease]
- Hereditary benign intraepithelial dyskeratosis [ICD-11 More detail]
Currated CISMeF NLP mapping
- Dyskeratosis, hereditary benign intraepithelial [OMIM Phenotype]
- Hereditary Benign Intraepithelial Dyskeratosis [NCIt concept]
- Hereditary benign intraepithelial dyskeratosis (disorder) [SNOMED CT concept]
- hereditary benign intraepithelial dyskeratosis [SNOMED Notion]
MeSH term(s) associated for indexing
- epithelium [MeSH Descriptor]
- skin abnormalities [MeSH Descriptor]
Record concept(s)
- dyskeratosis, hereditary benign intraepithelial [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dyskeratosis, hereditary benign intraepithelial [OMIM Phenotype]
- Hereditary Benign Intraepithelial Dyskeratosis [NCIt concept]
- Hereditary benign intraepithelial dyskeratosis [ORDO Disease]
- Hereditary benign intraepithelial dyskeratosis (disorder) [SNOMED CT concept]
- hereditary benign intraepithelial dyskeratosis [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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07/07/2025

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