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268298003: Turner's phenotype, other variant karyotypes (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    400961019 Turner's phenotype, other variant karyotypes en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    661022019 Turner's phenotype, other variant karyotypes (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    400961019 Turner's phenotype, other variant karyotypes en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    661022019 Turner's phenotype, other variant karyotypes (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    661022019 Turner's phenotype, other variant karyotypes (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Turner's phenotype, other variant karyotypes Is a Turner syndrome (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Turner's phenotype, other variant karyotypes Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Turner's phenotype, other variant karyotypes Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Turner's phenotype, other variant karyotypes Finding site Testis structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Turner's phenotype, other variant karyotypes Finding site Ovarian structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Turner's phenotype, other variant karyotypes Associated morphology Chromosomal morphology (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Turner's phenotype, other variant karyotypes Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Turner's phenotype, other variant karyotypes Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
    Turner's phenotype, other variant karyotypes Associated morphology Chromosomal morphology (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    WAS A association reference set (foundation metadata concept)

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