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

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

Origin ID

C567411;

UMLS CUI

C2677481;

Currated CISMeF NLP mapping
- Ectodermal Dysplasia and Immunodeficiency 2 [NCIt concept]
- Ectodermal dysplasia and immunodeficiency 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- Primary Immunodeficiency Diseases [MeSH Descriptor]
- ectodermal dysplasia [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
Record concept(s)
- ectodermal dysplasia, anhidrotic, with T-Cell immunodeficiency, autosomal dominant [MeSH 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]