MeSH Browser

MeSH Supplementary: Purpura simplex
Unique ID: C536249
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536249
Entry Term(s): Hereditary familial purpura simplex
Registry Numbers: 0
Heading Mapped to: *Purpura
Frequency: 20
Note: A form of purpura affecting the extremities. ECCHYMOSIS upon slight trauma and MENORRHAGIA are also common. OMIM: 179000
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Purpura simplex MeSH Supplementary Concept Data 2025