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26133007: Congenital atrophy (morphologic abnormality)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    43787010 Congenital atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
    756530014 Congenital atrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital atrophy Is a Congenital anomaly false Inferred relationship Existential restriction modifier
    Congenital atrophy Is a Atrophy false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Familial febrile convulsions Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 2
    Congenital cerebellar cortical atrophy Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 1
    Congenital atrophy of kidney Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 1
    Congenital ischemic atrophy of central nervous system structure Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 2
    Amyotrophia congenita Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 1
    Congenital cerebellar cortical atrophy Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 1
    Congenital atrophy of thyroid Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 1
    Congenital renal atrophy Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 1
    Congenital renal atrophy Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 1
    Congenital atrophy of thyroid Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 1
    Congenital cerebellar cortical atrophy Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 1
    Familial febrile convulsions Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 2
    Congenital cerebellar cortical atrophy Associated morphology False Congenital atrophy Inferred relationship Existential restriction modifier 1

    This concept is not in any reference sets

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