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424819008: Disorder due to cytochrome p450 enzyme variant (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2640206016 Disorder due to cytochrome p450 enzyme variant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2644260017 Disorder due to cytochrome p450 enzyme variant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2640206016 Disorder due to cytochrome p450 enzyme variant (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2640206016 Disorder due to cytochrome p450 enzyme variant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2644260017 Disorder due to cytochrome p450 enzyme variant en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2644260017 Disorder due to cytochrome p450 enzyme variant 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
    Disorder due to cytochrome p450 enzyme variant Is a Enzymopathy false Inferred relationship Existential restriction modifier (core metadata concept)

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Disorder due cytochrome p450 CYP2D6 variant Is a False Disorder due to cytochrome p450 enzyme variant Inferred relationship Existential restriction modifier (core metadata concept)
    Disorder due cytochrome p450 CYP2C9 variant Is a False Disorder due to cytochrome p450 enzyme variant Inferred relationship Existential restriction modifier (core metadata concept)
    Disorder due cytochrome p450 CYP2C19 variant Is a False Disorder due to cytochrome p450 enzyme variant Inferred relationship Existential restriction modifier (core metadata concept)
    Extensive metabolizer due to cytochrome p450 CYP2D6 variant Is a False Disorder due to cytochrome p450 enzyme variant Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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