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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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Whole chromosome trisomy, meiotic nondisjunction (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
    Whole chromosome trisomy, meiotic nondisjunction (disorder) localisation d'une constatation (attribut) Chromosome structure (cell structure) false Inferred relationship Some 1
    Whole chromosome trisomy, meiotic nondisjunction (disorder) est un(e) (attribut) Trisomy and partial trisomy of autosome false Inferred relationship Some
    Whole chromosome trisomy, meiotic nondisjunction (disorder) localisation d'une constatation (attribut) Chromosome structure (cell structure) false Inferred relationship Some 1
    Whole chromosome trisomy, meiotic nondisjunction (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
    Whole chromosome trisomy, meiotic nondisjunction (disorder) survenue (attribut) congénital false Inferred relationship Some 1
    Whole chromosome trisomy, meiotic nondisjunction (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique false Inferred relationship Some 1
    Whole chromosome trisomy, meiotic nondisjunction (disorder) localisation d'une constatation (attribut) Chromosome structure (cell structure) false Inferred relationship Some 1
    Whole chromosome trisomy, meiotic nondisjunction (disorder) survenue (attribut) congénital false Inferred relationship Some
    Whole chromosome trisomy, meiotic nondisjunction (disorder) morphologie associée (attribut) Alteration of chromosome structure false Inferred relationship Some
    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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