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1192004: Familial amyloid neuropathy, Finnish type (disorder)

    Status: retired, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3120012 Familial amyloid neuropathy, Finnish type en Synonym Active Initial character case insensitive SNOMED CT core
    3121011 Finnish type amyloidosis en Synonym Inactive Initial character case insensitive SNOMED CT core
    3122016 Meretoja type amyloidosis en Synonym Inactive Initial character case insensitive SNOMED CT core
    705455016 Familial amyloid neuropathy, Finnish type (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Familial amyloid neuropathy, Finnish type Is a Familial amyloid polyneuropathy false Inferred relationship Some
    Familial amyloid neuropathy, Finnish type Associated morphology Amyloid deposition false Inferred relationship Some 1
    Familial amyloid neuropathy, Finnish type Finding site Peripheral nervous system structure false Inferred relationship Some 1
    Familial amyloid neuropathy, Finnish type Finding site Peripheral nerve structure false Inferred relationship Some
    Familial amyloid neuropathy, Finnish type Finding site Nerve structure false Inferred relationship Some
    Familial amyloid neuropathy, Finnish type Associated morphology Amyloid deposition false Inferred relationship Some 1
    Familial amyloid neuropathy, Finnish type Finding site Peripheral nervous system structure false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Lattice corneal dystrophy Is a False Familial amyloid neuropathy, Finnish type Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set

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