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

254279009: Bonnevie-Ullrich syndrome NOS (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
    378513014 Bonnevie-Ullrich syndrome NOS en Synonym Active Entire term case sensitive SNOMED CT core module
    645149016 Bonnevie-Ullrich syndrome NOS (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
    Bonnevie-Ullrich syndrome NOS Is a Turner syndrome false Inferred relationship Existential restriction modifier
    Bonnevie-Ullrich syndrome NOS Finding site Testis structure false Inferred relationship Existential restriction modifier
    Bonnevie-Ullrich syndrome NOS Occurrence Congenital false Inferred relationship Existential restriction modifier
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Bonnevie-Ullrich syndrome NOS Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
    Bonnevie-Ullrich syndrome NOS Finding site Ovarian structure false Inferred relationship Existential restriction modifier
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Bonnevie-Ullrich syndrome NOS Associated morphology Chromosomal morphology false Inferred relationship Existential restriction modifier 2
    Bonnevie-Ullrich syndrome NOS Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
    Bonnevie-Ullrich syndrome NOS Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
    Bonnevie-Ullrich syndrome NOS 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