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402783001: Congenital/hereditary cutis laxa (disorder)


    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
    1770707019 Congenital/hereditary cutis laxa (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1781877014 Congenital/hereditary cutis laxa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    964451000052112 kongenital cutis laxa sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    kongenital cutis laxa Is a Cutis laxa false Inferred relationship Some
    kongenital cutis laxa Finding site Connective tissue structure false Inferred relationship Some
    kongenital cutis laxa Finding site Skin structure false Inferred relationship Some
    kongenital cutis laxa Occurrence Congenital false Inferred relationship Some
    kongenital cutis laxa Is a Congenital connective tissue disorder false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Cutis laxa secondary to inherited disorder of connective tissue (disorder) Is a False kongenital cutis laxa Inferred relationship Some
    SCARF syndrome Is a False kongenital cutis laxa Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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