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778061001: Familial cervical artery dissection (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2025. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3737582015 Familial cervical artery dissection (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3737583013 Familial cervical artery dissection en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3737584019 Hereditary cervical artery dissection en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3737585018 Hereditary CAD (cervical artery dissection) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3737586017 Familial CAD (cervical artery dissection) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3737587014 A rare genetic neurological disorder with characteristics of dissection of the cervical artery in various members of a single family, presenting with variable manifestations which range from asymptomatic to the triad of ipsilateral pain in the head, neck, and face, Horner syndrome and cerebral or retinal ischemic symptoms. Headache and cerebral ischemic features are most frequently observed. en Definition Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
    3737588016 A rare genetic neurological disorder with characteristics of dissection of the cervical artery in various members of a single family, presenting with variable manifestations which range from asymptomatic to the triad of ipsilateral pain in the head, neck, and face, Horner syndrome and cerebral or retinal ischaemic symptoms. Headache and cerebral ischaemic features are most frequently observed. en Definition Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
    5405595016 A rare genetic neurological disorder characterized by dissection of the cervical artery in various members of a single family, presenting with variable manifestations which range from asymptomatic to the triad of ipsilateral pain in the head, neck, and face, Horner syndrome, and cerebral or retinal ischemic symptoms. Headache and cerebral ischemic features are most frequently observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    5405596015 A rare genetic neurological disorder characterised by dissection of the cervical artery in various members of a single family, presenting with variable manifestations which range from asymptomatic to the triad of ipsilateral pain in the head, neck, and face, Horner syndrome, and cerebral or retinal ischaemic symptoms. Headache and cerebral ischaemic features are most frequently observed. en Definition 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
    Familial cervical artery dissection Is a Finding of head and neck region false Inferred relationship Some
    Familial cervical artery dissection Associated morphology Dissecting hemorrhage false Inferred relationship Some 1
    Familial cervical artery dissection Is a Arterial haemorrhage false Inferred relationship Some
    Familial cervical artery dissection Is a Familial disease false Inferred relationship Some
    Familial cervical artery dissection Finding site Cervical branch of vertebral artery false Inferred relationship Some 1
    Familial cervical artery dissection Is a Disease of non-coronary systemic artery false Inferred relationship Some
    Familial cervical artery dissection Is a Lesion of soft tissue (disorder) false Inferred relationship Some
    Familial cervical artery dissection Is a Cardiovascular system hereditary disorder false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Component annotation with string value reference set (foundation metadata concept)

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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