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28728008: autosomaal dominante polycysteuze nierziekte (aandoening)

    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
    48101017 Polycystic kidney disease, adult type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    48102012 Autosomal dominant adult polycystic kidney disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    483965010 Autosomal dominant polycystic kidney disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    483966011 ADPKD - Autosomal dominant polycystic kidney disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    483967019 Polycystic kidneys - adult type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    759440011 Polycystic kidney disease, adult type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    344351000146118 autosomaal dominante polycysteuze nierziekte [ADPKD] nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    344361000146115 autosomaal dominante polycysteuze nierziekte nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    344371000146114 autosomaal dominante polycysteuze nierziekte (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    autosomaal dominante polycysteuze nierziekte Is a Congenital cystic kidney disease false Inferred relationship Some
    autosomaal dominante polycysteuze nierziekte Is a Hereditary disorder of the urinary system false Inferred relationship Some
    autosomaal dominante polycysteuze nierziekte Is a Autosomal dominant hereditary disorder false Inferred relationship Some
    autosomaal dominante polycysteuze nierziekte Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 1
    autosomaal dominante polycysteuze nierziekte Finding site Urinary system structure (body structure) false Inferred relationship Some 9
    autosomaal dominante polycysteuze nierziekte Associated morphology Fibrocysticystic change (morphologic abnormality) false Inferred relationship Some 1
    autosomaal dominante polycysteuze nierziekte Course Multiple superficial injuries of lower leg false Inferred relationship Some
    autosomaal dominante polycysteuze nierziekte Occurrence Congenital false Inferred relationship Some
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 1
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 2
    autosomaal dominante polycysteuze nierziekte Associated morphology Fibrocystic change false Inferred relationship Some 2
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 1
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 1
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 2
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 1
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 1
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 2
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 2
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 1
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 1
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 2
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 1
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 2
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 1
    autosomaal dominante polycysteuze nierziekte Finding site Kidney structure false Inferred relationship Some 2
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Adult type polycystic kidney disease type 1 (disorder) Is a False autosomaal dominante polycysteuze nierziekte Inferred relationship Some
    Adult type polycystic kidney disease type 2 (disorder) Is a False autosomaal dominante polycysteuze nierziekte Inferred relationship Some
    Autosomal dominant polycystic kidney disease in childhood Is a False autosomaal dominante polycysteuze nierziekte Inferred relationship Some
    [EDTA] Polycystic kidneys, adult type (dominant) associated with renal failure Is a False autosomaal dominante polycysteuze nierziekte Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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