ectodermal dysplasia, anhidrotic, with T-Cell immunodeficiency, autosomal dominant

Preferred Label : ectodermal dysplasia, anhidrotic, with T-Cell immunodeficiency, autosomal dominant;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0567711;

UMLS CUI

C2677481;

Currated CISMeF NLP mapping
- Ectodermal Dysplasia and Immunodeficiency 2 [NCIt concept]
- Ectodermal dysplasia and immunodeficiency 2 [OMIM Phenotype]
Related record
- ectodermal dysplasia, anhidrotic, with T-Cell immunodeficiency, autosomal dominant [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ectodermal Dysplasia and Immunodeficiency 2 [NCIt concept]
- Ectodermal dysplasia and immunodeficiency 2 [OMIM Phenotype]

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