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125225005: Congenital malposition, right (morphologic abnormality)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2024. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    193715013 Congenital malposition, right en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    729023011 Congenital malposition, right (morphologic abnormality) en Fully specified name 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
    Congenital malposition, right Is a Congenital malposition false Inferred relationship Some
    Congenital malposition, right Is a Malposition (morphologic abnormality) false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Dextrotransposition of aorta (disorder) Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Mirror-imaged heart Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Dextrocardia Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Kartagener syndrome Associated morphology False Congenital malposition, right Inferred relationship Some 2
    Dextrokardie Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Mirror-imaged heart Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Dextrokardie Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Dextrocardia Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Kartagener syndrome Associated morphology False Congenital malposition, right Inferred relationship Some 2
    Dextrotransposition of aorta (disorder) Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Mirror-imaged heart Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Dextrokardie Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Spleen in right sided position (disorder) Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Dextrocardia Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Stomach in right sided position (disorder) Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Kartagener syndrome Associated morphology False Congenital malposition, right Inferred relationship Some 2
    A rare, congenital, non-syndromic, developmental defect during embryogenesis characterized by positioning of the heart in the right hemithorax, with the base and apex of the heart pointing caudally and to the right, due to abnormalities of embryologic origin that are intrinsic to the heart itself. Situs inversus or situs solitus may be associated, with extracardiac visceral transposition anomalies usually present in the former case and additional cardiac defects (e.g. septal defects, transposition of the great arteries, double-outlet right ventricle, anomalous pulmonary venous return, tetralogy of Fallot) frequently observed in both cases. Associated morphology False Congenital malposition, right Inferred relationship Some 1
    Complete situs inversus with dextrocardia Associated morphology False Congenital malposition, right Inferred relationship Some 1

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    REPLACED BY association reference set (foundation metadata concept)

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