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254279009: Bonnevie-Ullrich 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
    378513014 Bonnevie-Ullrich syndrome NOS en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    645149016 Bonnevie-Ullrich syndrome NOS (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    378513014 Bonnevie-Ullrich syndrome NOS en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    645149016 Bonnevie-Ullrich syndrome NOS (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    645149016 Bonnevie-Ullrich 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
    Bonnevie-Ullrich syndrome NOS Is a Turner syndrome (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Bonnevie-Ullrich syndrome NOS Finding site Testis structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Bonnevie-Ullrich syndrome NOS Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bonnevie-Ullrich syndrome NOS Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Bonnevie-Ullrich syndrome NOS Finding site Ovarian structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Bonnevie-Ullrich syndrome NOS Associated morphology Chromosomal morphology (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Bonnevie-Ullrich syndrome NOS Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Bonnevie-Ullrich syndrome NOS Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bonnevie-Ullrich syndrome NOS Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
    Bonnevie-Ullrich syndrome NOS Associated morphology Chromosomal morphology (morphologic abnormality) 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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