anhidrotic ectodermal dysplasia

Preferred Label : anhidrotic ectodermal dysplasia;

CISMeF synonym : Ectodermal Dysplasia, Anhidrotic;

UMLS semantic type : T019 - Congenital Abnormality;

Details

Origin ID

M0492746;

UMLS CUI

C1706004;

Currated CISMeF NLP mapping
- Anhidrotic ectodermal dysplasia [PASCAL descriptor]
- Anhidrotic ectodermal dysplasia [HPO term]
- Ectodermal dysplasia (anhidrotic) [ICD-10 Sub-category]
- Ectodermal dysplasia (anhidrotic) [ICD-10 Sub-category (who)]
- Hypohidrotic ectodermal dysplasia [ICD-11 Sub-sub category]
- Hypohidrotic ectodermal dysplasia [HPO term]
- Hypohidrotic ectodermal dysplasia [MedDRA LLT]
- Hypohidrotic ectodermal dysplasia [ORDO Disease]
- hypohidrotic ectodermal dysplasia [DO Concept]
Related record
- ectodermal dysplasia [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Anhidrotic ectodermal dysplasia [HPO term]
- Anhidrotic ectodermal dysplasia [PASCAL descriptor]
- Ectodermal dysplasia (anhidrotic) [ICD-10 Sub-category]
- Ectodermal dysplasia (anhidrotic) [ICD-10 Sub-category (who)]
Validated automatic mappings to BTNT
- Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) [SNOMED CT concept]
- Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive [OMIM Phenotype]
- Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive [OMIM Phenotype]
- hypohidrotic ectodermal dysplasia [Disease (Nov.)]

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