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190993005: Autosomal recessive severe combined immunodeficiency (disorder)

    Status: retired, Primitive. Date: 31-May 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    293692018 Autosomal recessive lymphopaenic agammaglobulinaemia en Synonym Active Case insensitive SNOMED CT core
    293693011 Autosomal recessive severe combined immunodeficiency en Synonym Active Case insensitive SNOMED CT core
    293694017 Autosomal recessive lymphopenic agammaglobulinemia en Synonym Active Case insensitive SNOMED CT core
    293695016 SCID - Autosomal recessive severe combined immunodeficiency en Synonym Active Case sensitive SNOMED CT core
    574640018 Autosomal recessive severe combined immunodeficiency (disorder) en Fully specified name Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Autosomal recessive severe combined immunodeficiency Pathological process Abnormal immune process false Inferred relationship Some 3
    Autosomal recessive severe combined immunodeficiency Is a Autosomal recessive hereditary disorder false Inferred relationship Some
    Autosomal recessive severe combined immunodeficiency Is a Severe combined immunodeficiency disease false Inferred relationship Some
    Autosomal recessive severe combined immunodeficiency Has definitional manifestation Immune system finding false Inferred relationship Some
    Autosomal recessive severe combined immunodeficiency Finding site Body system structure false Inferred relationship Some 2
    Autosomal recessive severe combined immunodeficiency Is a Autosomal recessive SCID (severe combined immunodeficiency disease) false Inferred relationship Some
    Autosomal recessive severe combined immunodeficiency Finding site Structure of immune system false Inferred relationship Some
    Autosomal recessive severe combined immunodeficiency Severity Severe false Inferred relationship Some
    Autosomal recessive severe combined immunodeficiency Occurrence Congenital false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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