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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:

    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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Histiocytic proliferation - category 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 Histiocytic proliferation - category Inferred relationship Some
    Histiocytosis Is a False Histiocytic proliferation - category Inferred relationship Some
    anémie hémolytique auto-immune avec érythrophagocytose (Fc portion de l'auto-anticorps) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Haemophagocytic lymphohistiocytosis Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Juvenile xanthogranuloma of iris Associated morphology False Histiocytic proliferation - category Inferred relationship Some 3
    Juvenile xanthogranuloma of skin (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 2
    Histiocytic syndrome Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Hemophagocytic syndrome Associated morphology False Histiocytic proliferation - category Inferred relationship Some
    Xanthogranuloma Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    [X]Other histiocytosis syndromes Associated morphology False Histiocytic proliferation - category Inferred relationship Some
    Xanthoma disseminatum (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 2
    Juvenile xanthogranuloma (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Multiple eruptive juvenile xanthogranuloma (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Non-Langerhans cell histiocytic dermatosis (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Cutaneous reticulohistiocytosis (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Solitary reticulohistiocytoma (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Diffuse normolipemic plane xanthomatosis (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Necrobiotic xanthogranuloma (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Necrobiotic xanthogranuloma with paraproteinemia (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Malakoplakia (involving skin) (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some
    Undetermined cell histiocytosis (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Macrophage activation syndrome (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 3
    Erdheim-Chester disease Associated morphology False Histiocytic proliferation - category Inferred relationship Some
    Xanthogranuloma of choroid plexus Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Erdheim-Chester disease (morphologic abnormality) Is a False Histiocytic proliferation - category Inferred relationship Some
    Chronic histiocytosis Associated morphology False Histiocytic proliferation - category Inferred relationship Some 2
    A rare cutaneous disease and a systemic inherited histiocytosis mainly characterised by hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, low height, and occasionally, hyperglycaemia/diabetes mellitus. Due to overlapping clinical features, it is now considered to include pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome (PHID), Faisalabad histiocytosis (FHC) and familial sinus histiocytosis with massive lymphadenopathy (FSHML). Some cases of dysosteosclerosis may also represent the syndrome. Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Hemophagocytic syndrome with human immunodeficiency virus infection (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 3
    Primary hemophagocytic lymphohistiocytosis Associated morphology False Histiocytic proliferation - category Inferred relationship Some 2
    Dermal dendritic cell histiocytosis Associated morphology False Histiocytic proliferation - category 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 Histiocytic proliferation - category 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 Histiocytic proliferation - category Inferred relationship Some 1
    A rare, secondary hemophagocytic lymphohistiocytosis characterized by occurring as either initial presentation of a malignant disease or at any stage during chemotherapy. The common associated malignancies are leukemias, 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 Histiocytic proliferation - category Inferred relationship Some 1
    Juvenile xanthogranuloma of iris Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Juvenile xanthogranuloma of skin (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Xanthogranuloma (morphologic abnormality) Is a False Histiocytic proliferation - category Inferred relationship Some
    Familial hemophagocytic lymphohistiocytosis (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 2
    Macrophage activation syndrome (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 2
    Hemophagocytic syndrome with human immunodeficiency virus infection (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Hemophagocytic lymphohistiocytosis due to infection (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 3
    Hemophagocytic lymphohistiocytosis due to malignant disease Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1
    Secondary hemophagocytic lymphohistiocytosis (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 2
    Solitary reticulohistiocytoma (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 2
    Cutaneous reticulohistiocytosis (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 2
    Macrophage activation syndrome due to juvenile systemic onset arthritis Associated morphology False Histiocytic proliferation - category Inferred relationship Some 3
    Hemophagocytic lymphohistiocytosis due to infection (disorder) Associated morphology False Histiocytic proliferation - category Inferred relationship Some 1

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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