histiocytosis, non-langerhans-cell

Preferred Label : histiocytosis, non-langerhans-cell;

MeSH definition : Group of disorders which feature accumulations of active HISTIOCYTES and LYMPHOCYTES, but where the histiocytes are not LANGERHANS CELLS. The group includes HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; SINUS HISTIOCYTOSIS; xanthogranuloma; reticulohistiocytoma; JUVENILE XANTHOGRANULOMA; xanthoma disseminatum; as well as the lipid storage diseases (SEA-BLUE HISTIOCYTE SYNDROME; and NIEMANN-PICK DISEASES).;

MeSH synonym : non-langerhans-cell histiocytosis; histiocytosis, non langerhans cell;

MeSH hyponym : xanthoma disseminatum; reticulohistiocytoma; Disseminatum, Xanthoma; Reticulohistiocytomas;

MeSH annotation : general or unspecified; prefer specifics;

Wikipedia link : https://en.wikipedia.org/wiki/Xanthoma disseminatum;

Details

Origin ID

D015616;

UMLS CUI

C0019624;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Deep histiocytoma (morphologic abnormality) [SNOMED CT concept]
- Disseminated xanthoma [MedDRA LLT]
- Langerhans Cell Histiocytosis [NCIt concept]
- Langerhans cell histiocytosis [PASCAL descriptor]
- Langerhans cell histiocytosis [Radlex concept]
- Langerhans cell histiocytosis [OMIM Phenotype]
- Langerhans cell histiocytosis [ORDO Disease]
- Langerhans cell histiocytosis (disorder) [SNOMED CT concept]
- Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype (morphologic abnormality) [Inactive SNOMED CT concept]
- Reticulohistiocytic granuloma (morphologic abnormality) [SNOMED CT concept]
- Reticulohistiocytoma [ICD-11 Extension code]
- Xanthoma disseminatum [ICD-11 More detail]
- Xanthoma disseminatum [ORDO Disease]
- Xanthoma disseminatum (disorder) [SNOMED CT concept]
- diffuse xanthoma [SNOMED Notion]
- reticulohistiocytic granuloma [DO Concept]
- xanthoma disseminatum [Radlex concept]
Currated CISMeF NLP mapping
- Hemophagocytic syndrome (disorder) [Inactive SNOMED CT concept]
- Non langerhans cell histiocytosis [PASCAL descriptor]
- Non-Langerhans cell histiocytosis [ORDO Disease]
- non langerhans cell histiocytosis [Disease (Nov.)]
- non-Langerhans cell histiocytosis [Radlex concept]
- non-Langerhans-cell histiocytosis [DO Concept]
DO Cross reference
- non-Langerhans-cell histiocytosis [DO Concept]
- reticulohistiocytic granuloma [DO Concept]
Manual BTNT mappings - CISMeF
- Benign cephalic histiocytosis [ORDO Disease]
- Hereditary progressive mucinous histiocytosis [ORDO Disease]
- Indeterminate cell histiocytosis [ORDO Disease]
- Necrobiotic xanthogranuloma [ORDO Disease]
- Papular xanthoma [ORDO Disease]
- Progressive nodular histiocytosis [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Other acquired skin disease [ORDO Disease]
- Rare systemic disease [ORDO Disease]
ORDO relation(s)
- Non-Langerhans cell histiocytosis [ORDO Disease]
Record concept(s)
- histiocytosis, Non-Langerhans-Cell [MeSH concept]
- reticulohistiocytoma [MeSH concept]
- xanthoma disseminatum [MeSH concept]
See also inter- (CISMeF)
- Primary haemophagocytic lymphohistiocytosis [ICD-11 Sub-sub category]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Non-Langerhans cell histiocytosis [ORDO Disease]
- non-Langerhans cell histiocytosis [Radlex concept]
- non-Langerhans-cell histiocytosis [DO Concept]

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