skin diseases, genetic

Preferred Label : skin diseases, genetic;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0019934;

UMLS CUI

C0037277;

Currated CISMeF NLP mapping
- Congenital anomaly of skin (disorder) [SNOMED CT concept]
- congenital anomaly of skin, nos [SNOMED Notion]
Related record
- skin diseases, genetic [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Genodermatosis [NCIt concept]
- Genodermatosis (disorder) [SNOMED CT concept]
- Rare genetic skin disease [ORDO Disease]
- genodermatosis [Disease (Nov.)]