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1285323003: Inverse Klippel Trénaunay syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2025. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    5246547019 Inverse Klippel Trénaunay syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    5246548012 Inverse Klippel Trénaunay syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    5246549016 A rare vascular anomaly with the association of capillary and venous malformations with hypotrophy or shortening of an affected limb due to alterations in bones, muscles, or subcutaneous tissues. In most cases, at least one of the findings is noted shortly after birth, while the other components become evident later in infancy. en Definition Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
    5400758016 A rare vascular anomaly characterized by the association of capillary and venous malformations with hypotrophy or shortening of an affected limb due to alterations in bones, muscles, or subcutaneous tissues. In most cases, at least one of the findings is noted shortly after birth, while the other components become evident later in infancy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    5400759012 A rare vascular anomaly characterised by the association of capillary and venous malformations with hypotrophy or shortening of an affected limb due to alterations in bones, muscles, or subcutaneous tissues. In most cases, at least one of the findings is noted shortly after birth, while the other components become evident later in infancy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Inverse Klippel Trénaunay syndrome Is a Capillary-venous malformation false Inferred relationship Some
    Inverse Klippel Trénaunay syndrome Is a Multiple malformation syndrome with limb defect as major feature false Inferred relationship Some
    Inverse Klippel Trénaunay syndrome Is a Longitudinal deficiency of limb false Inferred relationship Some
    Inverse Klippel Trénaunay syndrome Occurrence Congenital false Inferred relationship Some 1
    Inverse Klippel Trénaunay syndrome Finding site Entire limb false Inferred relationship Some 1
    Inverse Klippel Trénaunay syndrome Associated morphology Abnormally short false Inferred relationship Some 1
    Inverse Klippel Trénaunay syndrome Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Inverse Klippel Trénaunay syndrome Occurrence Congenital false Inferred relationship Some 2
    Inverse Klippel Trénaunay syndrome Finding site Structure of capillary blood vessel false Inferred relationship Some 2
    Inverse Klippel Trénaunay syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 2
    Inverse Klippel Trénaunay syndrome Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
    Inverse Klippel Trénaunay syndrome Occurrence Congenital false Inferred relationship Some 3
    Inverse Klippel Trénaunay syndrome Finding site Venous structure false Inferred relationship Some 3
    Inverse Klippel Trénaunay syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 3
    Inverse Klippel Trénaunay syndrome Pathological process (attribute) Pathological developmental process false Inferred relationship Some 3
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Component annotation with string value reference set (foundation metadata concept)

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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