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93355005: Congenital malposition of tail (disorder)


    Status: retired, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    154508015 Congenital malposition of tail en Synonym Active Case insensitive SNOMED CT core
    154509011 Congenital malpositioned tail en Synonym Active Case insensitive SNOMED CT core
    837071013 Congenital malposition of tail (disorder) en Fully specified name Active Case insensitive SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital malposition of tail Finding site Tail structure false Inferred relationship Some 1
    Congenital malposition of tail Finding site Tail structure false Inferred relationship Some 1
    Congenital malposition of tail Finding site Tail structure false Inferred relationship Some 2
    Congenital malposition of tail Finding site Tail structure false Inferred relationship Some 1
    Congenital malposition of tail Finding site Non-human body structure false Inferred relationship Some
    Congenital malposition of tail Is a Congenital abnormality of lower limb and pelvic girdle false Inferred relationship Some
    Congenital malposition of tail Is a Congenital anomaly of animal tail false Inferred relationship Some
    Congenital malposition of tail Associated morphology Congenital malposition false Inferred relationship Some 1
    Congenital malposition of tail Finding site Tail structure false Inferred relationship Some 1
    Congenital malposition of tail Finding site Tail structure false Inferred relationship Some 2
    Congenital malposition of tail Finding site Tail structure false Inferred relationship Some 1
    Congenital malposition of tail Associated morphology Developmental abnormality false Inferred relationship Some 2
    Congenital malposition of tail Associated morphology Congenital malposition false Inferred relationship Some 1
    Congenital malposition of tail Occurrence Congenital false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    MOVED TO association reference set

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