Erythema palmare hereditarium

Preferred Label : Erythema palmare hereditarium;

Type : Phenotype or locus, molecular basis unknown;

Description : Erythema palmare hereditarium is a benign condition that was first described by Lane (1929). Erythema usually presents at birth and remains stable throughout life. Histology shows dilated vessels in the entire dermis with inflammatory infiltrate. Capillaroscopy reveals an increased number of capillary loops running parallel to the surface (summary by Kluger and Guillot, 2010).;

Inheritance : Autosomal dominant;

Prefixed ID : %133000;

Details

Origin ID

133000;

UMLS CUI

C1851502;

Currated CISMeF NLP mapping
- Erythema palmare hereditarium [ORDO Disease]
- Erythema palmare hereditarium (disorder) [SNOMED CT concept]
- erythema palmare hereditarium [MeSH concept]
- erythema palmare hereditarium [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Erythema [HPO term]
ORDO concept(s)
- Erythema palmare hereditarium [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Erythema palmare hereditarium [ORDO Disease]
- Erythema palmare hereditarium (disorder) [SNOMED CT concept]
- erythema palmare hereditarium [MeSH Supplementary Concept]
- erythema palmare hereditarium [MeSH concept]

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