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205529007: Amyotrophica congenita (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2003. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    315183011 Amyotrophica congenita en Synonym Active Entire term case sensitive SNOMED CT core module
    590911019 Amyotrophica congenita (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
    Amyotrophica congenita Is a Congenital anomaly of skeletal muscle false Inferred relationship Existential restriction modifier
    Amyotrophica congenita Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier
    Amyotrophica congenita Occurrence Congenital false Inferred relationship Existential restriction modifier
    Amyotrophica congenita Is a Disorder of skeletal muscle false Inferred relationship Existential restriction modifier
    Amyotrophica congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier

    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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