414414006: Histiocytic proliferation - category (morphologic abnormality)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Histiocytær proliferation	Is a	Proliferation of hematopoietic cell type (morphologic abnormality)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Histiocytic neoplasm (morphology)	Is a	False	Histiocytær proliferation	Inferred relationship	Some
Histiocytosis	Is a	False	Histiocytær proliferation	Inferred relationship	Some
Hemolytic erythrophagocytic syndrome	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Haemophagocytic lymphohistiocytosis	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Juvenile xanthogranuloma of iris	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	3
Juvenile xanthogranuloma of skin (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	2
Histiocytic syndrome	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Hæmofagocytosesyndrom	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some
Xanthogranuloma	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
[X]Other histiocytosis syndromes	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some
Xanthoma disseminatum (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	2
Juvenile xanthogranuloma (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Multiple eruptive juvenile xanthogranuloma (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Non-Langerhans cell histiocytic dermatosis (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Cutaneous reticulohistiocytosis (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Solitary reticulohistiocytoma (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Diffuse normolipemic plane xanthomatosis (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Necrobiotic xanthogranuloma (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Necrobiotic xanthogranuloma with paraproteinemia (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Malakoplakia (involving skin) (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some
Undetermined cell histiocytosis (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Macrophage activation syndrome (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	3
Erdheim-Chester disease	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some
Xanthogranuloma of choroid plexus	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Erdheim-Chester disease (morphologic abnormality)	Is a	False	Histiocytær proliferation	Inferred relationship	Some
Chronic histiocytosis	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	2
A rare cutaneous disease and a systemic inherited histiocytosis with main characteristics of hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, low height, and occasionally, hyperglycaemia/diabetes mellitus. The syndrome becomes clinically apparent mostly during childhood, but cases during infancy and late-onset cases have been reported too. Caused by mutations in SLC29A3 (10q22.2) (encoding a nucleoside transporter, hENT3), which result in defective nucleoside transport functions of hENT3. This leads to histiocytic infiltration of numerous organs. Transmission is autosomal recessive.	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Hemophagocytic syndrome with human immunodeficiency virus infection (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	3
Primary hemophagocytic lymphohistiocytosis	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	2
Dermal dendritic cell histiocytosis	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Papular xanthoma is a form of non-Langerhans cell histiocytosis characterized by cutaneous presentation of solitary or disseminated yellow to orange-brown papular or papulonodular, noncoalescent, asymptomatic skin lesions located predominantly on the head, neck, trunk and extremities (rarely on oral mucosa), in the presence of normolipidemia. Microscopically, the lesions consist of monomorphous infiltrate of xanthomatous macrophages and numerous Touton giant cells, with scant or absent inflammatory infiltrate. It is usually not associated with systemic disease.	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Progressive nodular histiocytosis is a rare, normolipemic, non-Langerhans cell histiocytosis characterized by progressive growth of multiple to disseminated, asymptomatic skin lesions that range in appearance from yellow plaques to coalescence-prone red-brown papules, nodules and pedunculated tumors up to 5 cm in size, located typically on the face, trunk and extremities (and rarely on conjunctiva and mucous membranes). Characteristic microscopic findings include a storiform spindle cell infiltrate in the deep dermis with xanthomatous macrophages and some Touton cells in the upper dermis. It is usually not associated with systemic disease.	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
A rare secondary haemophagocytic lymphohistiocytosis characterised by occurring as either initial presentation of a malignant disease or at any stage during chemotherapy. The common associated malignancies are leukaemias, B-cell, T-cell or NK-cell lymphomas, and Hodgkin lymphoma. Typical clinical manifestation includes fever, hepatosplenomegaly and cytopenias, combined with specific laboratory findings.	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Juvenile xanthogranuloma of iris	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Juvenile xanthogranuloma of skin (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Xanthogranuloma (morphologic abnormality)	Is a	False	Histiocytær proliferation	Inferred relationship	Some
Familial hemophagocytic lymphohistiocytosis (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	2
Macrophage activation syndrome (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	2
Hemophagocytic syndrome with human immunodeficiency virus infection (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Hemophagocytic lymphohistiocytosis due to infection (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	3
Hemophagocytic lymphohistiocytosis due to malignant disease	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1
Secondary hemophagocytic lymphohistiocytosis (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	2
Solitary reticulohistiocytoma (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	2
Cutaneous reticulohistiocytosis (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	2
Macrophage activation syndrome due to juvenile systemic onset arthritis	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	3
Hemophagocytic lymphohistiocytosis due to infection (disorder)	Associated morphology	False	Histiocytær proliferation	Inferred relationship	Some	1

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
2530944017	Histiocytic proliferation - category (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2534411010	Histiocytic proliferation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2537358012	Histiocytic proliferation - category	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2544641000005115	Histiocytær proliferation	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)