Multifocal and multisystemic (disseminated) Langerhans-cell histiocytosis

Preferred Label : Multifocal and multisystemic (disseminated) Langerhans-cell histiocytosis;

Inclusion CIM-10 : Histiocytosis X, multisystemic; Letterer-Siwe disease;

ICD-10 exclusion note : adult pulmonary Langerhans cell histiocytosis (J84.82); unifocal Langerhans-cell histiocytosis (C96.6); multifocal and unisystemic Langerhans-cell histiocytosis (C96.5);

Diag associé à un acte (%) : 90.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

C960;

UMLS CUI

C2861649;

Automatic exact mappings (from CISMeF team)
- Langerhans cell histiocytosis, disseminated (morphologic abnormality) [SNOMED CT concept]
- Langerhans-cell histiocytosis [DO Concept]
- Letterer-Siwe disease [ICD-11 Extension code]
- Letterer-Siwe disease [ICD-11 Extension code]
- histiocytosis, Langerhans-Cell [MeSH Descriptor]
Currated CISMeF NLP mapping
- Langerhans cell histiocytosis, disseminated (disorder) [SNOMED CT concept]
- Letterer-Siwe Disease [NCIt concept]
- Letterer-Siwe disease [Radlex concept]
- Letterer-Siwe disease [ORDO Disease]
- Letterer-Siwe disease [MedDRA LLT]
- Letterer-siwe disease [OMIM Phenotype]
DO Cross reference
- Langerhans-cell histiocytosis [DO Concept]
Excluded by
- Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue [ICD-10 category]
Orphanet concepts
- Langerhans cell histiocytosis [ORDO Disease]
- Letterer-Siwe disease [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
Validated automatic mappings to NTBT
- langerhans cell histiocytosis [Disease (Nov.)]

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