MeSH Browser

MeSH Supplementary: Hyper-IgM Immunodeficiency, X-Linked, with Ectodermal Dysplasia, Hypohidrotic
Unique ID: C564542
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564542
Entry Term(s): Xhm-Ed
Registry Numbers: 0
Heading Mapped to: *Ectodermal Dysplasia; *Hyper-IgM Immunodeficiency Syndrome, Type 1
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Hyper-IgM Immunodeficiency, X-Linked, with Ectodermal Dysplasia, Hypohidrotic MeSH Supplementary Concept Data 2025