hidrotic ectodermal dysplasia syndrome

Preferred Label : hidrotic ectodermal dysplasia syndrome;

Détails

Origin ID

D4-01104;

UMLS CUI

C0162361;

Automatic exact mappings (from CISMeF team)
- Hidrotic ectodermal dysplasia [PASCAL descriptor]
CISMeF manual mappings
- Hidrotic ectodermal dysplasia [HPO term]
Currated CISMeF NLP mapping
- Clouston syndrome [DO Concept]
- Clouston syndrome [OMIM Phenotype]
- Clouston syndrome [MedDRA LLT]
- Hidrotic ectodermal dysplasia [ORDO Disease]
- Hidrotic ectodermal dysplasia [MedDRA LLT]
- Hidrotic ectodermal dysplasia syndrome (disorder) [SNOMED CT concept]
- hidrotic ectodermal dysplasia [MeSH concept]
False UMLS correspondences (reviewed by CISMeF team)
- ectodermal dysplasia [MeSH Descriptor]
False automatic mappings
- ectodermal dysplasia [MeSH Descriptor]
ICD-10 exact mapping(s)
- Ectodermal dysplasia (anhidrotic) [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature [ORDO Disease]
- Ectodermal dysplasia syndrome [ORDO Disease]
- Hereditary palmoplantar keratoderma [ORDO Disease]
- Zlotogura-Martinez syndrome [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Hidrotic ectodermal dysplasia syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Clouston syndrome [OMIM Phenotype]
- Clouston syndrome [MedDRA LLT]
- Clouston syndrome [DO Concept]
- Hidrotic ectodermal dysplasia [ORDO Disease]
- Hidrotic ectodermal dysplasia [MedDRA LLT]
- Hidrotic ectodermal dysplasia [HPO term]
- Hidrotic ectodermal dysplasia syndrome (disorder) [SNOMED CT concept]
- hidrotic ectodermal dysplasia [MeSH concept]

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