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205719003: 46, XX true hermaphrodite (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    315485011 46, XX true hermaphrodite en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    591125012 46, XX true hermaphrodite (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1696681000005116 46, XX ægte hermafrodit da Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Danish module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    46, XX ægte hermafrodit Is a Congenital disorder due to abnormality of chromosome number OR structure (disorder) false Inferred relationship Some
    46, XX ægte hermafrodit Is a Hermafroditisme false Inferred relationship Some
    46, XX ægte hermafrodit Is a Congenital anomaly of endocrine gland false Inferred relationship Some
    46, XX ægte hermafrodit Occurrence Congenital false Inferred relationship Some
    46, XX ægte hermafrodit Finding site Entire endocrine gonad (body structure) false Inferred relationship Some
    46, XX ægte hermafrodit Associated morphology Alteration of chromosome structure false Inferred relationship Some
    46, XX ægte hermafrodit Finding site Gonadal endocrine structure false Inferred relationship Some 2
    46, XX ægte hermafrodit Finding site Chromosome structure false Inferred relationship Some 1
    46, XX ægte hermafrodit Associated morphology kongenit anomali false Inferred relationship Some 1
    46, XX ægte hermafrodit Associated morphology kongenit anomali false Inferred relationship Some
    46, XX ægte hermafrodit Finding site Chromosome structure false Inferred relationship Some 1
    46, XX ægte hermafrodit Occurrence Congenital false Inferred relationship Some 1
    46, XX ægte hermafrodit Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
    46, XX ægte hermafrodit Finding site Chromosome structure false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    GB English

    US English

    REPLACED BY association reference set (foundation metadata concept)

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