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205987003: [X]Chromosomal abnormalities, not elsewhere classified (disorder)

    Status: retired, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2638235013 [X]Chromosomal abnormalities, not elsewhere classified (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
    2642304013 [X]Chromosomal abnormalities, not elsewhere classified en Synonym Active Initial character case insensitive SNOMED CT core
    315797011 [X]Chromosomal abnormalities, not elswhere classified en Synonym Inactive Initial character case insensitive SNOMED CT core
    591427014 [X]Chromosomal abnormalities, not elswhere classified (disorder) en Fully specified name Inactive Case sensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    [X]Chromosomal abnormalities, not elsewhere classified Associated morphology Alteration of chromosome structure false Inferred relationship Some
    [X]Chromosomal abnormalities, not elsewhere classified Occurrence Congenital false Inferred relationship Some
    [X]Chromosomal abnormalities, not elsewhere classified Associated morphology Congenital anomaly false Inferred relationship Some 1
    [X]Chromosomal abnormalities, not elsewhere classified Finding site Chromosome structure false Inferred relationship Some 1
    [X]Chromosomal abnormalities, not elsewhere classified Associated morphology Congenital anomaly false Inferred relationship Some 1
    [X]Chromosomal abnormalities, not elsewhere classified Finding site Chromosome structure false Inferred relationship Some 1
    [X]Chromosomal abnormalities, not elsewhere classified Is a Congenital chromosomal disease false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    MOVED TO association reference set

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