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Marie Unna congenital hypotrichosis MeSH Supplementary Concept Data 2024


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 Number
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 Preferred
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