MeSH Browser

MeSH Supplementary: Total Hypotrichosis, Mari type
Unique ID: C536973
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536973
Entry Term(s): Alopecia Universalis Congenita, Mari type; Hypotrichosis, Autosomal Recessive; Hypotrichosis, Localized, Autosomal Recessive, 2; Hypotrichosis, Total, Mari Type; Mari type Alopecia universalis congenita
Registry Numbers: 0
Heading Mapped to: Alopecia / congenital
Frequency: 6
Note: Lah2 not included
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Total Hypotrichosis, Mari type MeSH Supplementary Concept Data 2025