purpura simplex

Preferred Label : purpura simplex;

MeSH synonym : hereditary familial purpura simplex;

Origin ID

C536249;

UMLS CUI

C0272309;

Automatic exact mappings (from CISMeF team)
- Capillaritis [ICD-11 Subcategory]
- Other nonthrombocytopenic purpura [ICD-10 Sub-category]
- Other nonthrombocytopenic purpura [ICD-10 Sub-category (who)]
- Purpura simplex [MedDRA LLT]
Currated CISMeF NLP mapping
- Purpura simplex [OMIM Phenotype]
- Purpura simplex (disorder) [SNOMED CT concept]
- purpura simplex [SNOMED Notion]
MeSH term(s) associated for indexing
- purpura [MeSH Descriptor]
Record concept(s)
- Purpura simplex [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Purpura simplex [OMIM Phenotype]
- Purpura simplex [MedDRA LLT]
- Purpura simplex (disorder) [SNOMED CT concept]
- purpura simplex [SNOMED Notion]