MeSH Browser

MeSH Supplementary: Congenital alopecia X-linked
Unique ID: C535981
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535981
Entry Term(s): Alopecia congenital; Alopecia, Congenital; Congenital alopecia
Registry Number: 0
Heading Mapped to: *Alopecia; *Genetic Diseases, X-Linked
Frequency: 33
Note: Congenital cases of alopecia that exhibit X-linked inheritance. OMIM: 300042
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Concept UI: M0530442
Registry Number: 0
Terms: Congenital alopecia X-linked Preferred Term
Term UI T737871
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Alopecia congenital
Term UI T737873
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Alopecia, Congenital
Term UI T800930
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Congenital alopecia
Term UI T737872
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Congenital alopecia X-linked MeSH Supplementary Concept Data 2024