familial Letterer-Siwe disease

Preferred Label : familial Letterer-Siwe disease;

MeSH synonym : histiocytosis X, acute disseminated;

Origin ID

C538636;

UMLS CUI

C5779774;

Automatic exact mappings (from CISMeF team)
- Letterer-siwe disease [OMIM Phenotype]
DO Cross reference
- Langerhans-cell histiocytosis [DO Concept]
MeSH term(s) associated for indexing
- histiocytosis, Langerhans-Cell [MeSH Descriptor]
ORDO relation(s)
- Letterer-Siwe disease [ORDO Disease]
Record concept(s)
- Familial Letterer-Siwe disease [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Langerhans cell histiocytosis, disseminated [ICD-O code]
- Langerhans cell histiocytosis, disseminated (disorder) [SNOMED CT concept]
- Langerhans cell histiocytosis, disseminated (morphologic abnormality) [SNOMED CT concept]
- Letterer-Siwe Disease [NCIt concept]
- Letterer-Siwe disease [ICD-10 Sub-category (who)]
- Letterer-Siwe disease [MedDRA LLT]
- Letterer-Siwe disease [ORDO Disease]
- Letterer-Siwe disease [ICD-9 code]
- Letterer-Siwe disease [Radlex concept]
- Letterer-siwe disease [OMIM Phenotype]