FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

423163008: Disorder due cytochrome p450 CYP2D6 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
    2640207013 Disorder due cytochrome p450 CYP2D6 variant (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2644261018 Disorder due cytochrome p450 CYP2D6 variant en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    999931000052113 sjukdom orsakad av cytokrom P450, variant CYP2D6 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 CYP2D6 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 CYP2D6 Is a False sjukdom orsakad av cytokrom P450, variant CYP2D6 Inferred relationship Some
    intermediär metaboliserare på grund av cytokrom P450, variant CYP2D6 Is a False sjukdom orsakad av cytokrom P450, variant CYP2D6 Inferred relationship Some
    extensiv metaboliserare på grund av cytokrom P450, variant CYP2D6 Is a False sjukdom orsakad av cytokrom P450, variant CYP2D6 Inferred relationship Some
    ultrarapid metaboliserare på grund av cytokrom P450, variant CYP2D6 Is a False sjukdom orsakad av cytokrom P450, variant CYP2D6 Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

    Back to Start