Pigmented purpuric eruption

Preferred Label : Pigmented purpuric eruption;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant; ? same as Schamberg disease;

Prefixed ID : %172900;

Details

Origin ID

172900;

UMLS CUI

C0406515;

Automatic exact mappings (from CISMeF team)
- Pigmented purpuric lichenoid dermatitis of Gougerot and Blum (disorder) [SNOMED CT concept]
- pigmentation disorders [MeSH Descriptor]
Currated CISMeF NLP mapping
- Familial pigmented purpuric eruption (disorder) [SNOMED CT concept]
- pigmented purpuric eruption [MeSH concept]
- pigmented purpuric eruption [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the skin [HPO term]
- Autosomal dominant inheritance [HPO term]
- Neonatal onset [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial pigmented purpuric eruption (disorder) [SNOMED CT concept]
- pigmented purpuric eruption [MeSH Supplementary Concept]
- pigmented purpuric eruption [MeSH concept]

Keyword's position in hierarchy(ies) :

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