Hyper-IgM immunodeficiency, X-Linked, with ectodermal dysplasia, hypohidrotic

Preferred Label : Hyper-IgM immunodeficiency, X-Linked, with ectodermal dysplasia, hypohidrotic;

MeSH synonym : Xhm-Ed;

Origin ID

C564542;

UMLS CUI

C1846008;

Currated CISMeF NLP mapping
- Ectodermal Dysplasia and Immunodeficiency 1 [NCIt concept]
- Ectodermal dysplasia and immunodeficiency 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- Hyper-IgM immunodeficiency syndrome, type 1 [MeSH Descriptor]
- ectodermal dysplasia [MeSH Descriptor]
Record concept(s)
- Hyper-IgM immunodeficiency, X-Linked, with ectodermal dysplasia, hypohidrotic [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ectodermal Dysplasia and Immunodeficiency 1 [NCIt concept]
- Ectodermal dysplasia and immunodeficiency 1 [OMIM Phenotype]