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205656002: Whole chromosome trisomy, meiotic nondisjunction (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    315398015 Whole chromosome trisomy, meitotic nondisjunction en Synonym Inactive Only initial character case insensitive SNOMED CT core module
    591054015 Whole chromosome trisomy, meitotic nondisjunction (disorder) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
    2718984015 Whole chromosome trisomy, meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    2770276013 Whole chromosome trisomy, meiotic nondisjunction en Synonym Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Whole chromosome trisomy, meiotic nondisjunction Is a Trisomy and partial trisomy of autosome false Inferred relationship Existential restriction modifier
    Whole chromosome trisomy, meiotic nondisjunction Occurrence Congenital false Inferred relationship Existential restriction modifier
    Whole chromosome trisomy, meiotic nondisjunction Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
    Whole chromosome trisomy, meiotic nondisjunction Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Whole chromosome trisomy, meiotic nondisjunction Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
    Whole chromosome trisomy, meiotic nondisjunction Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
    Whole chromosome trisomy, meiotic nondisjunction Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
    Whole chromosome trisomy, meiotic nondisjunction Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Whole chromosome trisomy, meiotic nondisjunction Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
    Whole chromosome trisomy, meiotic nondisjunction Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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