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11884006: Congenital hyperrotation (morphologic abnormality)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    20497014 Congenital hyperrotation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    701891013 Congenital hyperrotation (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    20497014 Congenital hyperrotation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    20497014 Congenital hyperrotation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    701891013 Congenital hyperrotation (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    701891013 Congenital hyperrotation (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 hyperrotation Is a Congenital malrotation false Inferred relationship Existential restriction modifier (core metadata concept)

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital curled tail Associated morphology False Congenital hyperrotation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital curled tail Associated morphology False Congenital hyperrotation Inferred relationship Existential restriction modifier (core metadata concept) 1

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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