FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

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

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

    Descriptions:

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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Turner's phenotype, other variant karyotypes Is a Turner syndrome false Inferred relationship Existential restriction modifier
    Turner's phenotype, other variant karyotypes Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
    Turner's phenotype, other variant karyotypes Occurrence Congenital false Inferred relationship Existential restriction modifier
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Turner's phenotype, other variant karyotypes Finding site Testis structure false Inferred relationship Existential restriction modifier
    Turner's phenotype, other variant karyotypes Finding site Ovarian structure false Inferred relationship Existential restriction modifier
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Turner's phenotype, other variant karyotypes Associated morphology Chromosomal morphology false Inferred relationship Existential restriction modifier 2
    Turner's phenotype, other variant karyotypes Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Turner's phenotype, other variant karyotypes Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Turner's phenotype, other variant karyotypes Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
    Turner's phenotype, other variant karyotypes Associated morphology Chromosomal morphology false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start