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205639005: Whole chromosome monosomy, mosaicism NOS (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    315378013 Whole chromosome monosomy, mosaicism NOS en Synonym Active Initial character case insensitive SNOMED CT core
    591036019 Whole chromosome monosomy, mosaicism 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
    Whole chromosome monosomy, mosaicism NOS Associated morphology Alteration of chromosome structure false Inferred relationship Some
    Whole chromosome monosomy, mosaicism NOS Occurrence Congenital false Inferred relationship Some
    Whole chromosome monosomy, mosaicism NOS Finding site Chromosome structure false Inferred relationship Some 1
    Whole chromosome monosomy, mosaicism NOS Associated morphology Congenital anomaly false Inferred relationship Some 1
    Whole chromosome monosomy, mosaicism NOS Finding site Chromosome structure false Inferred relationship Some 1
    Whole chromosome monosomy, mosaicism NOS Associated morphology Congenital anomaly false Inferred relationship Some
    Whole chromosome monosomy, mosaicism NOS Is a Whole chromosome monosomy - mitotic nondisjunction mosaicism 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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