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26133007: Congenital atrophy (morphologic abnormality)


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

    Descriptions:

    Id Description Lang Type Status Case? Module
    43787010 Congenital atrophy en Synonym Active Case insensitive SNOMED CT core
    756530014 Congenital atrophy (morphologic abnormality) 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 atrophy Is a Congenital anomaly false Inferred relationship Some
    Congenital atrophy Is a Atrophy false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital cerebellar cortical atrophy Associated morphology False Congenital atrophy Inferred relationship Some 1
    Congenital atrophy of thyroid Associated morphology False Congenital atrophy Inferred relationship Some 1
    Congenital renal atrophy Associated morphology False Congenital atrophy Inferred relationship Some 1
    Congenital renal atrophy Associated morphology False Congenital atrophy Inferred relationship Some 1
    Congenital atrophy of thyroid Associated morphology False Congenital atrophy Inferred relationship Some 1
    Congenital cerebellar cortical atrophy Associated morphology False Congenital atrophy Inferred relationship Some 1
    Familial febrile convulsions Associated morphology False Congenital atrophy Inferred relationship Some 2
    Congenital cerebellar cortical atrophy Associated morphology False Congenital atrophy Inferred relationship Some 1
    Familial febrile convulsions Associated morphology False Congenital atrophy Inferred relationship Some 2
    Congenital cerebellar cortical atrophy Associated morphology False Congenital atrophy Inferred relationship Some 1
    Congenital atrophy of kidney Associated morphology False Congenital atrophy Inferred relationship Some 1
    Congenital ischaemic atrophy of central nervous system structure Associated morphology False Congenital atrophy Inferred relationship Some 2
    Amyotrophia congenita Associated morphology False Congenital atrophy Inferred relationship Some 1

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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