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425191003: Disorder due cytochrome p450 CYP2C19 variant (disorder)


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

    Descriptions:

    Id Description Lang Type Status Case? Module
    2640209011 Disorder due cytochrome p450 CYP2C19 variant (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2644263015 Disorder due cytochrome p450 CYP2C19 variant en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    975751000052112 sjukdom orsakad av cytokrom P450, variant CYP2C19 sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    sjukdom orsakad av cytokrom P450, variant CYP2C19 Is a sjukdom orsakad av variant av enzymet cytokrom P450 false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    långsam metaboliserare på grund av cytokrom P450, variant CYP2C19 Is a False sjukdom orsakad av cytokrom P450, variant CYP2C19 Inferred relationship Some
    intermediär metaboliserare på grund av cytokrom p450, variant CYP2C19 Is a False sjukdom orsakad av cytokrom P450, variant CYP2C19 Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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