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205701007: Klinefelter's syndrome NOS (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
    315465012 Klinefelter's syndrome NOS en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    591105013 Klinefelter's syndrome NOS (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    315465012 Klinefelter's syndrome NOS en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    591105013 Klinefelter's syndrome NOS (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    591105013 Klinefelter's syndrome NOS (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
    Klinefelter's syndrome NOS Is a A male with two or more X chromosomes. false Inferred relationship Existential restriction modifier (core metadata concept)
    Klinefelter's syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Klinefelter's syndrome NOS Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Klinefelter's syndrome NOS Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Klinefelter's syndrome NOS Is a Klinefelter's syndrome false Inferred relationship Existential restriction modifier (core metadata concept)
    Klinefelter's syndrome NOS Is a Klinefelter's syndrome - male with more than two X chromosomes false Inferred relationship Existential restriction modifier (core metadata concept)
    Klinefelter's syndrome NOS Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Klinefelter's syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Klinefelter's syndrome NOS Associated morphology anomalie congénitale 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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