MeSH Browser

MeSH Supplementary: Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant
Unique ID: C567411
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567411
Registry Numbers: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)
Heading Mapped to: *Ectodermal Dysplasia; *Primary Immunodeficiency Diseases
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2019/06/17

Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant MeSH Supplementary Concept Data 2025