FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  FHIR Version n/a  User: [n/a]

1192004: Familial amyloid neuropathy, Finnish type (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

    Descriptions:

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

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

    This concept is not in any reference sets

    Back to Start