Other histiocytosis syndromes

Preferred Label : Other histiocytosis syndromes;

Inclusion CIM-10 : Reticulohistiocytoma (giant-cell); Xanthogranuloma; Sinus histiocytosis with massive lymphadenopathy;

Diag associé à un acte (%) : 87.9;

Source : OMS;

Date de début : 01/01/1997;

Détails

Origin ID

D763;

UMLS CUI

C0477320;

Automatic exact mappings (from CISMeF team)
- Cutaneous Adult Xanthogranuloma [NCIt concept]
- Histiocytosis-lymphadenopathy plus syndrome [OMIM Phenotype]
- Lipogranuloma (morphologic abnormality) [SNOMED CT concept]
- Reactive Xanthogranuloma [NCIt concept]
- Rosai Dorfman disease [PASCAL descriptor]
- Rosai-Dorfman-Destombes Disease [NCIt concept]
- Rosaï-Dorfman disease [ORDO Disease]
- Sinus histiocytosis with massive lymphadenopathy [ICD-11 More detail]
- Sinus histiocytosis with massive lymphadenopathy (disorder) [SNOMED CT concept]
- Xanthogranuloma [MedDRA Preferred Term]
- Xanthogranuloma [PASCAL descriptor]
- Xanthogranuloma (disorder) [SNOMED CT concept]
- Xanthogranuloma (morphologic abnormality) [SNOMED CT concept]
- histiocytosis, sinus [MeSH Descriptor]
- histiocytosis-lymphadenopathy plus syndrome [DO Concept]
Orphanet concepts
- Benign cephalic histiocytosis [ORDO Disease]
- Erdheim-Chester disease [ORDO Disease]
- Faisalabad histiocytosis [ORDO Disease]
- Familial sinus histiocytosis with massive lymphadenopathy [ORDO Disease]
- Generalized eruptive histiocytosis [ORDO Disease]
- H syndrome [ORDO Disease]
- Hereditary progressive mucinous histiocytosis [ORDO Disease]
- Indeterminate cell histiocytosis [ORDO Disease]
- Juvenile xanthogranuloma [ORDO Disease]
- Multicentric reticulohistiocytosis [ORDO Disease]
- Necrobiotic xanthogranuloma [ORDO Disease]
- Non-Langerhans cell histiocytosis [ORDO Disease]
- Papular xanthoma [ORDO Disease]
- Progressive nodular histiocytosis [ORDO Disease]
- Rosaï-Dorfman disease [ORDO Disease]
- Sea-blue histiocytosis [ORDO Disease]
- Systemic non-Langerhans cell histiocytosis [ORDO Disease]
- Xanthoma disseminatum [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- Diseases of immune dysregulation [ICD-11 Subcategory]

Position du mot-clé dans l'(les) arborescence(s) :

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