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58404005: Congenital impairment (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
    97060018 Congenital impairment en Synonym Active Entire term case insensitive SNOMED CT core module
    797133016 Congenital impairment (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 impairment Is a Congenital anomaly false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Partial congenital impairment Is a False Congenital impairment Inferred relationship Existential restriction modifier
    Total congenital impairment Is a False Congenital impairment Inferred relationship Existential restriction modifier
    Congenital anomaly of ear with impairment of hearing Associated morphology False Congenital impairment Inferred relationship Existential restriction modifier 1
    Congenital absence of auricle with atresia of auditory canal Associated morphology False Congenital impairment Inferred relationship Existential restriction modifier 1
    Congenital absence of auricle with stenosis of auditory canal Associated morphology False Congenital impairment Inferred relationship Existential restriction modifier 1
    Congenital absence of external ear Associated morphology False Congenital impairment Inferred relationship Existential restriction modifier 2
    Congenital absence of external ear, unspecified Associated morphology False Congenital impairment Inferred relationship Existential restriction modifier 1
    Earpit syndrome Associated morphology False Congenital impairment Inferred relationship Existential restriction modifier 1
    Jervell and Lange-Nielsen syndrome Associated morphology False Congenital impairment Inferred relationship Existential restriction modifier 2
    Jervell and Lange-Nielson syndrome Associated morphology False Congenital impairment Inferred relationship Existential restriction modifier 2

    This concept is not in any reference sets

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