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205656002: Whole chromosome trisomy, meiotic nondisjunction (disorder)


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

    Descriptions:

    Id Description Lang Type Status Case? Module
    2718984015 Whole chromosome trisomy, meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2770276013 Whole chromosome trisomy, meiotic nondisjunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2480511000052117 trisomi för hel kromosom, meiotisk icke-disjunktion sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    trisomi för hel kromosom, meiotisk icke-disjunktion Is a Trisomy and partial trisomy of autosome false Inferred relationship Some
    trisomi för hel kromosom, meiotisk icke-disjunktion Occurrence Congenital false Inferred relationship Some
    trisomi för hel kromosom, meiotisk icke-disjunktion Associated morphology Alteration of chromosome structure false Inferred relationship Some
    trisomi för hel kromosom, meiotisk icke-disjunktion Associated morphology kongenital anomali false Inferred relationship Some 1
    trisomi för hel kromosom, meiotisk icke-disjunktion Finding site Chromosome structure false Inferred relationship Some 1
    trisomi för hel kromosom, meiotisk icke-disjunktion Finding site Chromosome structure false Inferred relationship Some 1
    trisomi för hel kromosom, meiotisk icke-disjunktion Associated morphology kongenital anomali false Inferred relationship Some
    trisomi för hel kromosom, meiotisk icke-disjunktion Occurrence Congenital false Inferred relationship Some 1
    trisomi för hel kromosom, meiotisk icke-disjunktion Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 1
    trisomi för hel kromosom, meiotisk icke-disjunktion Finding site Chromosome structure false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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