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205441002: Klippel-Feil syndrome NOS (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    315016011 Klippel-Feil syndrome NOS en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    590807014 Klippel-Feil syndrome NOS (disorder) en Fully specified name 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
    Klippel-Feil syndrome NOS Is a Klippel-Feil sequence false Inferred relationship Some
    Klippel-Feil syndrome NOS Finding site Bone structure of cervical vertebra false Inferred relationship Some 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 2
    Klippel-Feil syndrome NOS Finding site Spinal cord structure false Inferred relationship Some 2
    Klippel-Feil syndrome NOS Occurrence Congenital false Inferred relationship Some
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 2
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 2
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 2
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 2
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Some 2

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    WAS A association reference set

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