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419398009: Meretoja syndrome (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
    2574191011 Meretoja syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2577530013 Meretoja syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2580142018 Amyloid cranial neuropathy with lattice corneal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2580146015 Meretoja type amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    998561000052119 familjär amyloid polyneuropati typ 5 sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    familjär amyloid polyneuropati typ 5 Is a Corneal deposit false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Is a Chromosomal disorder (disorder) false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Is a Systemic amyloidosis false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Is a Disorder of soft tissue of head false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Is a Soft tissue lesion false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Is a Neuropathy (disorder) false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Is a Disorder of connective tissue (disorder) false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Finding site Structure of substantia propria of cornea false Inferred relationship Some 1
    familjär amyloid polyneuropati typ 5 Finding site Chromosome structure false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Associated morphology Amyloid deposition false Inferred relationship Some 1
    familjär amyloid polyneuropati typ 5 Finding site Nerve structure false Inferred relationship Some 1
    familjär amyloid polyneuropati typ 5 Is a Corneal stroma finding false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Is a Ocular amyloid deposit false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Finding site Nerve structure false Inferred relationship Some 1
    familjär amyloid polyneuropati typ 5 Associated morphology Amyloid deposition false Inferred relationship Some 1
    familjär amyloid polyneuropati typ 5 Finding site Structure of substantia propria of cornea false Inferred relationship Some 1
    familjär amyloid polyneuropati typ 5 Finding site Chromosome structure false Inferred relationship Some 2
    familjär amyloid polyneuropati typ 5 Is a Corneal stromal degeneration (disorder) false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Associated morphology Amyloid deposition false Inferred relationship Some 2
    familjär amyloid polyneuropati typ 5 Is a Hereditary amyloidosis (disorder) false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Is a Hereditary disorder of the visual system (disorder) false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Is a Autosomal dominant hereditary disorder false Inferred relationship Some
    familjär amyloid polyneuropati typ 5 Finding site Structure of substantia propria of cornea false Inferred relationship Some 2
    familjär amyloid polyneuropati typ 5 Is a Hereditary disorder of nervous system false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    kornealdystrofi, lattice, typ 2 Is a False familjär amyloid polyneuropati typ 5 Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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