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233745009: Defect of diaphragm (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2023. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    350249011 Defect of diaphragm en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    621971011 Defect of diaphragm (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
    Defect of diaphragm Is a Disorder of diaphragm (disorder) false Inferred relationship Some
    Defect of diaphragm Finding site Diaphragm structure false Inferred relationship Some
    Defect of diaphragm Finding site Entire body wall (body structure) false Inferred relationship Some
    Defect of diaphragm Finding site Body wall structure false Inferred relationship Some
    Defect of diaphragm Is a Lesion of soft tissue (disorder) false Inferred relationship Some
    Defect of diaphragm Associated morphology Defect false Inferred relationship Some 1
    Defect of diaphragm Finding site Diaphragm structure false Inferred relationship Some 1
    Defect of diaphragm Is a Lesion of skeletal muscle (disorder) false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital eventration of diaphragm Is a False Defect of diaphragm Inferred relationship Some
    Diaphragmatic hernia Is a False Defect of diaphragm Inferred relationship Some
    Congenital absence of diaphragm Is a False Defect of diaphragm Inferred relationship Some
    Aplasia of diaphragm (disorder) Is a False Defect of diaphragm Inferred relationship Some
    A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by diaphragmatic hernia, lung hypoplasia, ossification defect of the skull, and severe limb hypoplasia. Other clinical features may include, syndactyly, clinodactyly, extra spleen, absence of the femur or pelvic bone, partial intestinal malrotation, omphalocele and testicular atrophy. Is a False Defect of diaphragm Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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