FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

205441002: Klippel-Feil syndrome NOS (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    315016011 Klippel-Feil syndrome NOS en Synonym Active Entire term case sensitive SNOMED CT core module
    590807014 Klippel-Feil syndrome NOS (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

    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 Existential restriction modifier
    Klippel-Feil syndrome NOS Finding site Bone structure of cervical vertebra false Inferred relationship Existential restriction modifier 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 2
    Klippel-Feil syndrome NOS Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 2
    Klippel-Feil syndrome NOS Occurrence Congenital false Inferred relationship Existential restriction modifier
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 2
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 2
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 2
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 2
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 1
    Klippel-Feil syndrome NOS Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start