FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

128809007: Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype (morphologic abnormality)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    207339017 Langerhans cell histiocytosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2774275015 Langerhans cell histiocytosis, no ICD-O subtype en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2973189011 Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype (morphologic abnormality) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2973251014 Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype en Synonym (core metadata concept) 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
    Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Is a Histiocytic neoplasm (morphologic abnormality) false Inferred relationship Some
    Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Is a Neoplasm of uncertain behaviour false Inferred relationship Some
    Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Is a Langerhans cell histiocytosis - category false Inferred relationship Some
    Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Is a Malignant histiocytic neoplasm - category false Inferred relationship Some
    Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Is a Malignant histiocytic neoplasm (morphologic abnormality) false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Pulmonary histiocytosis X Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Eosinophilic granuloma of bone Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some 1
    Langerhans cell histiocytosis, disseminated (disorder) Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Eosinophilic granuloma Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Pulmonary eosinophilic granuloma Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Hand-Schüller-Christian disease Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Langerhans cell histiocytosis Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Gastrointestinal eosinophilic granuloma Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Eosinophilic granuloma of oral mucosa Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Letterer-Siwe disease of intra-abdominal lymph nodes Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Letterer-Siwe disease of intrapelvic lymph nodes Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Letterer-Siwe disease of intrathoracic lymph nodes Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    gedissemineerde Langerhans-cel-histiocytose van lymfeklier van axilla en/of bovenste extremiteit Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Langerhans-cel-histiocytose van lymfeklieren van hoofd-halsregio Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    gedissemineerde Langerhans-cel-histiocytose van lymfeklier van regio inguinalis en/of onderste extremiteit Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Letterer-Siwe disease of lymph nodes of multiple sites Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Letterer-Siwe disease of spleen Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    gedissemineerde Langerhans-cel-histiocytose met extranodale lokalisatie en/of lokalisatie in solide orgaan Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Letterer-Siwe disease of lymph nodes of head, face and neck Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Letterer-Siwe disease of lymph nodes of axilla and upper limb Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Letterer-Siwe disease of lymph nodes of inguinal region and lower limb Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some 1
    Langerhan's cell histiocytosis Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Langerhans cell histiocytosis, disseminated (clinical) Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Langerhans cell histiocytosis, unifocal, bone Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Letterer-Siwe disease Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Letterer-Siwe disease of unspecified sites Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Letterer-Siwe disease NOS Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some
    Langerhans cell histiocytosis - Hashimoto-Pritzker type (disorder) Associated morphology False Langerhans cell histiocytosis, no International Classification of Diseases for Oncology subtype Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

    Back to Start