MeSH Browser

MeSH Supplementary: Marie Unna congenital hypotrichosis
Unique ID: C535912
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535912
Entry Term(s): Hypotrichosis, Marie Unna type; Marie Unna hereditary hypotrichosis
Registry Numbers: 0
Heading Mapped to: Hypotrichosis / congenital
Frequency: 17
Note: Congenital hypotrichosis characterized by little or no eyebrows, eyelashes, or body hair at birth, followed by the development of coarse, wiry, twisted hair in early childhood which progresses to ALOPECIA. Two genetically distinct forms exist; type I is caused by mutations in the hair growth associated (HR) gene. OMIM: 146550
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Marie Unna congenital hypotrichosis MeSH Supplementary Concept Data 2025