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780841002: leucémie mastocytaire classique (trouble)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    1009541000172112 leucémie mastocytaire classique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
    3743927017 Classic mast cell leukemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3743928010 Classic mast cell leukaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3743929019 Classic mast cell leukemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    785481000241114 leucémie mastocytaire classique (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
    3743930012 A very rare aggressive form of systemic mastocytosis characterised by abnormal growth and proliferation of neoplastic mast cells (>20%) in the bone marrow and/or blood, as well as other tissues such as the liver, peritoneum, spleen or bones. Patients typically present with symptoms related to mast cell activation (for example hot flushes, fever, malaise, diarrhoea, tachycardia), weight loss, anorexia and hepatosplenomegaly or less frequently cutaneous mastocytosis. Gastroduodenal ulcers (often complicated by haemorrhage), ascites and portal hypertension have also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3743931011 A very rare aggressive form of systemic mastocytosis characterized by abnormal growth and proliferation of neoplastic mast cells (>20%) in the bone marrow and/or blood, as well as other tissues such as the liver, peritoneum, spleen or bones. Patients typically present with symptoms related to mast cell activation (for example hot flushes, fever, malaise, diarrhea, tachycardia), weight loss, anorexia and hepatosplenomegaly or less frequently cutaneous mastocytosis. Gastroduodenal ulcers (often complicated by hemorrhage), ascites and portal hypertension have also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    leucémie mastocytaire classique morphologie associée (attribut) Mast cell leukemia false Inferred relationship Some 1
    leucémie mastocytaire classique localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some 1
    leucémie mastocytaire classique est un(e) (attribut) Systemic mast cell disease (disorder) false Inferred relationship Some
    leucémie mastocytaire classique est un(e) (attribut) Mast cell leukemia (clinical) false Inferred relationship Some
    leucémie mastocytaire classique Pathological process (attribute) Abnormal immune process (qualifier value) false Inferred relationship Some 2
    leucémie mastocytaire classique localisation d'une constatation (attribut) Mast cell false Inferred relationship Some 3
    leucémie mastocytaire classique est un(e) (attribut) Leukaemia false Inferred relationship Some
    leucémie mastocytaire classique est un(e) (attribut) néoplasme des mastocytes false Inferred relationship Some
    leucémie mastocytaire classique morphologie associée (attribut) Hyperplasia (morphologic abnormality) false Inferred relationship Some 3
    leucémie mastocytaire classique est un(e) (attribut) Malignant white blood cell disorder false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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