MeSH Browser

MeSH Supplementary: T-cell immunodeficiency, congenital alopecia and nail dystrophy
Unique ID: C536781
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536781
Entry Term(s): Congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency; Pignata Guarino syndrome; T-Cell Immunodeficiency, Congenital Alopecia, And Nail Dystrophy
Registry Numbers: 0
Heading Mapped to: *Alopecia; *Nail Diseases; *Severe Combined Immunodeficiency
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2012/12/03

T-cell immunodeficiency, congenital alopecia and nail dystrophy MeSH Supplementary Concept Data 2025