MeSH Browser

MeSH Supplementary: Pigmented purpuric eruption
Unique ID: C537186
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537186
Entry Term(s): Familial Schamberg's disease; Familial pigmented purpuric eruption; Schamberg purpura
Registry Number: 0
Heading Mapped to: *Pigmentation Disorders; *Purpura
Frequency: 26
Note: Pigmented purpura that are present from birth or infancy, usually in a bilaterally symmetric pattern on the lower extermities. OMIM: 172900
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Concept UI: M0531647
Registry Number: 0
Terms: Pigmented purpuric eruption Preferred Term
Term UI T741751
Date02/24/2009
LexicalTag NON
ThesaurusID; Schamberg purpura
Term UI T741753
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Familial Schamberg's disease
Term UI T753805
Date07/02/2009
LexicalTag NON
ThesaurusID ORD (2010); Familial pigmented purpuric eruption
Term UI T741752
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Pigmented purpuric eruption MeSH Supplementary Concept Data 2024