histiocytosis, familial lipochrome

Preferred Label : histiocytosis, familial lipochrome;

Origin ID

C562738;

UMLS CUI

C0334125;

Currated CISMeF NLP mapping
- Histiocytosis, familial lipochrome [OMIM Phenotype]
- Lipochrome histiocytosis - familial (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- genetic diseases, inborn [MeSH Descriptor]
- histiocytosis [MeSH Descriptor]
Record concept(s)
- histiocytosis, familial lipochrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Histiocytosis, familial lipochrome [OMIM Phenotype]
- Lipochrome histiocytosis (morphologic abnormality) [SNOMED CT concept]
- Lipochrome histiocytosis - familial (disorder) [SNOMED CT concept]
- lipochrome histiocytosis [SNOMED Notion]