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230561007: Congenital neuropathy with arthrogryposis multiplex congenita (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    345473013 Congenital neuropathy with arthrogryposis multiplex congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    618388015 Congenital neuropathy with arthrogryposis multiplex congenita (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    345473013 Congenital neuropathy with arthrogryposis multiplex congenita en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    345473013 Congenital neuropathy with arthrogryposis multiplex congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    618388015 Congenital neuropathy with arthrogryposis multiplex congenita (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    618388015 Congenital neuropathy with arthrogryposis multiplex congenita (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
    Congenital neuropathy with arthrogryposis multiplex congenita Is a polyneuropathie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital neuropathy with arthrogryposis multiplex congenita Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Finding site Nerve structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital neuropathy with arthrogryposis multiplex congenita Is a Neuropathy false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital neuropathy with arthrogryposis multiplex congenita Is a Congenital anomaly of the peripheral nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Congenital neuropathy with arthrogryposis multiplex congenita Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Congenital neuropathy with arthrogryposis multiplex congenita Is a Congenital anomaly of joint false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Contracture false Inferred relationship Existential restriction modifier (core metadata concept) 5
    Congenital neuropathy with arthrogryposis multiplex congenita Finding site Joint structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
    Congenital neuropathy with arthrogryposis multiplex congenita Is a Arthrogryposis false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Finding site Joint structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Finding site Nerve structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Contracture false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital neuropathy with arthrogryposis multiplex congenita Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital neuropathy with arthrogryposis multiplex congenita Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital neuropathy with arthrogryposis multiplex congenita Interprets Range of joint movement false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Congenital neuropathy with arthrogryposis multiplex congenita Has interpretation Decreased false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Congenital neuropathy with arthrogryposis multiplex congenita Finding site Structure of joint region false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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