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276266002: Disorder of bilirubin metabolism and excretion (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2006. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    412337016 Disorder of bilirubin metabolism and excretion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    669160010 Disorder of bilirubin metabolism and excretion (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2244581000005118 Forstyrrelse af bilirubinstofskifte og -udskillelse da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Forstyrrelse af bilirubinstofskifte og -udskillelse Is a Disorder of porphyrin and heme metabolism false Inferred relationship Some
    Forstyrrelse af bilirubinstofskifte og -udskillelse Finding site Body system structure false Inferred relationship Some
    Forstyrrelse af bilirubinstofskifte og -udskillelse Occurrence Congenital false Inferred relationship Some
    Forstyrrelse af bilirubinstofskifte og -udskillelse Is a Disorder of porphyrin metabolism false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    nordamerikansk indiansk intrahepatisk kolestase Is a False Forstyrrelse af bilirubinstofskifte og -udskillelse Inferred relationship Some
    Benign recurrent intrahepatic cholestasis Is a False Forstyrrelse af bilirubinstofskifte og -udskillelse Inferred relationship Some
    Inherited disorder of bilirubin metabolism Is a False Forstyrrelse af bilirubinstofskifte og -udskillelse Inferred relationship Some
    Familial arthrogryposis-cholestatic hepatorenal syndrome Is a False Forstyrrelse af bilirubinstofskifte og -udskillelse Inferred relationship Some
    A heterogeneous group of autosomal recessive disorders of childhood that disrupt bile formation and present with cholestasis of hepatocellular origin. Three types of PFIC have been identified and are related to mutations in hepatocellular transport system genes involved in bile formation. Main clinical manifestations include cholestasis, pruritus and jaundice. Is a False Forstyrrelse af bilirubinstofskifte og -udskillelse Inferred relationship Some
    Disorders of bilirubin excretion Is a False Forstyrrelse af bilirubinstofskifte og -udskillelse Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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