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268229003: Indeterminate sex and pseudohermaphroditism (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    400865010 Indeterminate sex and pseudohermaphroditism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    400866011 Gynandrism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    660944018 Indeterminate sex and pseudohermaphroditism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2241281000005118 ubestemmeligt køn og pseudohermafroditisme da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    ubestemmeligt køn og pseudohermafroditisme Is a Congenital malformation of genital organs false Inferred relationship Some
    ubestemmeligt køn og pseudohermafroditisme Occurrence Congenital false Inferred relationship Some
    ubestemmeligt køn og pseudohermafroditisme Finding site Genital structure false Inferred relationship Some 1
    ubestemmeligt køn og pseudohermafroditisme Course Multiple superficial injuries of lower leg false Inferred relationship Some
    ubestemmeligt køn og pseudohermafroditisme Associated morphology kongenit anomali false Inferred relationship Some 1
    ubestemmeligt køn og pseudohermafroditisme Associated morphology Kongenit malformation false Inferred relationship Some 1
    ubestemmeligt køn og pseudohermafroditisme Occurrence Congenital false Inferred relationship Some
    ubestemmeligt køn og pseudohermafroditisme Associated morphology Kongenit malformation false Inferred relationship Some 1
    ubestemmeligt køn og pseudohermafroditisme Finding site Genital structure false Inferred relationship Some 1
    ubestemmeligt køn og pseudohermafroditisme Occurrence Congenital false Inferred relationship Some 2
    ubestemmeligt køn og pseudohermafroditisme Associated morphology dysgenese false Inferred relationship Some 2
    ubestemmeligt køn og pseudohermafroditisme Finding site Genital structure false Inferred relationship Some 2
    ubestemmeligt køn og pseudohermafroditisme Occurrence Congenital false Inferred relationship Some 1
    ubestemmeligt køn og pseudohermafroditisme Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    ubestemmeligt køn og pseudohermafroditisme Associated morphology Morphologically abnormal structure false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Ovotestis Is a False ubestemmeligt køn og pseudohermafroditisme Inferred relationship Some
    Pseudohermaphroditism Is a False ubestemmeligt køn og pseudohermafroditisme Inferred relationship Some
    Pure gonadal dysgenesis Is a False ubestemmeligt køn og pseudohermafroditisme Inferred relationship Some
    False hermaphrodite Is a False ubestemmeligt køn og pseudohermafroditisme Inferred relationship Some
    ubestemmeligt køn eller pseudohermafroditisme, ikke nærmere specificeret Is a False ubestemmeligt køn og pseudohermafroditisme Inferred relationship Some
    Ubestemmeligt køn, ikke nærmere specificeret Is a False ubestemmeligt køn og pseudohermafroditisme Inferred relationship Some
    Pseudohermafrodit, ikke nærmere specificeret Is a False ubestemmeligt køn og pseudohermafroditisme Inferred relationship Some
    Meacham syndrome is a multiple malformation syndrome characterized by congenital diaphragmatic abnormalities, genital defects and cardiac malformations. Is a False ubestemmeligt køn og pseudohermafroditisme Inferred relationship Some
    46,XY ovotesticular disorder of sex development is a rare, genetic disorder of sex development characterized by either the coexistence of both male and female reproductive gonads or, more frequently, by the presence of one or both gonads containing a mixture of both testicular and ovarian tissue (ovotestes) in an individual with a normal male 46, XY karyotype. External genitalia are usually ambiguous but can range from normal male to normal female and if a uterus and/or fallopian tubes are present, they are generally hypoplastic. Cryptorchidism, hypospadias, infertility and increased risk of gonadal tumors are frequently associated. Is a False ubestemmeligt køn og pseudohermafroditisme Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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