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105987004: Malformation defect spectrum (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    170406013 Malformation defect spectrum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    576971014 Malformation defect spectrum (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Malformation defect spectrum Is a Multiple congenital malformations false Inferred relationship Some
    Malformation defect spectrum Occurrence Congenital false Inferred relationship Some
    Malformation defect spectrum Associated morphology Congenital malformation false Inferred relationship Some
    Malformation defect spectrum Occurrence Congenital false Inferred relationship Some 1
    Malformation defect spectrum Is a Congenital malformation syndrome (disorder) false Inferred relationship Some
    Malformation defect spectrum Associated morphology anomalie du développement false Inferred relationship Some 1
    Malformation defect spectrum Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
    Malformation defect spectrum Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Facio-auriculo-vertebral spectrum (disorder) Is a False Malformation defect spectrum Inferred relationship Some
    A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies). Is a False Malformation defect spectrum Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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