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703220002: Hereditary cystatin C amyloid angiopathy (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    3007478010 Hereditary cystatin C amyloid angiopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3007920011 Hereditary cystatin C amyloid angiopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3008060012 A rare fatal amyloid disease in young people caused by a mutation in cystatin C. This condition predisposes towards intracerebral haemorrhage and dementia and is inherited in a dominant pattern. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3008067010 A rare fatal amyloid disease in young people caused by a mutation in cystatin C. This condition predisposes towards intracerebral hemorrhage and dementia and is inherited in a dominant pattern. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3007478010 Hereditary cystatin C amyloid angiopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3007920011 Hereditary cystatin C amyloid angiopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3008060012 A rare fatal amyloid disease in young people caused by a mutation in cystatin C. This condition predisposes towards intracerebral haemorrhage and dementia and is inherited in a dominant pattern. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3008067010 A rare fatal amyloid disease in young people caused by a mutation in cystatin C. This condition predisposes towards intracerebral hemorrhage and dementia and is inherited in a dominant pattern. 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
    Hereditary cystatin C amyloid angiopathy Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary cystatin C amyloid angiopathy Is a Cerebral amyloid angiopathy false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary cystatin C amyloid angiopathy Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary cystatin C amyloid angiopathy Is a Cardiovascular system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary cystatin C amyloid angiopathy Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary cystatin C amyloid angiopathy Finding site Cerebrovascular system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary cystatin C amyloid angiopathy Is a Hereditary amyloidosis (disorder) 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)

    SAME AS association reference set (foundation metadata concept)

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