Phrynoderma - CISMeF

Preferred Label : Phrynoderma;

NCIt definition : Rough, dry, hypertrophic eruption of the skin associated with vitamin A deficiency.;

Origin ID

C112827;

UMLS CUI

C0334013;

Automatic exact mappings (from CISMeF team)
- Phrynoderma [PASCAL descriptor]
- Phrynoderma [ICD-11 More detail]
- Phrynoderma (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Follicular hyperkeratosis [HPO term]
- Follicular hyperkeratosis (disorder) [SNOMED CT concept]
- Follicular hyperkeratosis (morphologic abnormality) [SNOMED CT concept]
- Phrynoderma [PASCAL descriptor]
- Phrynoderma (disorder) [SNOMED CT concept]
- follicular hyperkeratosis [SNOMED Notion]
- phrynoderma [Disease (Nov.)]