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205729005: Conditions due to anomaly of unspecified chromosome NOS (disorder)

    Status: retired, Primitive. Date: 31-Jan 2010. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    315495016 Conditions due to anomaly of unspecified chromosome NOS en Synonym Active Initial character case insensitive SNOMED CT core
    591136017 Conditions due to anomaly of unspecified chromosome NOS (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Conditions due to anomaly of unspecified chromosome NOS Occurrence Congenital false Inferred relationship Some
    Conditions due to anomaly of unspecified chromosome NOS Associated morphology Alteration of chromosome structure false Inferred relationship Some
    Conditions due to anomaly of unspecified chromosome NOS Associated morphology Congenital anomaly false Inferred relationship Some 1
    Conditions due to anomaly of unspecified chromosome NOS Finding site Chromosome structure false Inferred relationship Some 1
    Conditions due to anomaly of unspecified chromosome NOS Associated morphology Congenital anomaly false Inferred relationship Some
    Conditions due to anomaly of unspecified chromosome NOS Finding site Chromosome structure false Inferred relationship Some 1
    Conditions due to anomaly of unspecified chromosome NOS Is a Other condition due to autosomal anomaly false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Australian dialect reference set

    Concept inactivation indicator reference set

    WAS A association reference set

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