melanin pigmentation, nos

Preferred Label : melanin pigmentation, nos;

Origin ID

M-57200;

UMLS CUI

C0333617;

Automatic exact mappings (from CISMeF team)
- MART-1 antigen [MeSH concept]
- melanosis [MeSH Descriptor]
- melanosis [MeSH concept]
Currated CISMeF NLP mapping
- Melanin pigmentation (morphologic abnormality) [SNOMED CT concept]
Décrit
- infantile melanodontia [SNOMED Notion]
- melanoplakia [SNOMED Notion]
SNOMED CT concept
- Melanin pigmentation (morphologic abnormality) [SNOMED CT concept]
Semantic type(s)
- Organ or Tissue Function [UMLS semantic type]
UMLS correspondences (same concept)
- Melanin pigmentation (morphologic abnormality) [SNOMED CT concept]