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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
    3564841000005117 familliær amyloid polyneuropati, type V da Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Danish module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    familliær amyloid polyneuropati, type V Is a Corneal deposit false Inferred relationship Some
    familliær amyloid polyneuropati, type V Is a Chromosomal disorder (disorder) false Inferred relationship Some
    familliær amyloid polyneuropati, type V Is a Systemic amyloidosis false Inferred relationship Some
    familliær amyloid polyneuropati, type V Is a Disorder of soft tissue of head false Inferred relationship Some
    familliær amyloid polyneuropati, type V Is a Lesion of soft tissue (disorder) false Inferred relationship Some
    familliær amyloid polyneuropati, type V Is a Neuropathy (disorder) false Inferred relationship Some
    familliær amyloid polyneuropati, type V Is a Disorder of connective tissue (disorder) false Inferred relationship Some
    familliær amyloid polyneuropati, type V Finding site Structure of substantia propria of cornea false Inferred relationship Some 1
    familliær amyloid polyneuropati, type V Finding site Chromosome structure false Inferred relationship Some
    familliær amyloid polyneuropati, type V Associated morphology Amyloid deposition false Inferred relationship Some 1
    familliær amyloid polyneuropati, type V Finding site Nerve structure false Inferred relationship Some 1
    familliær amyloid polyneuropati, type V Is a Corneal stroma finding false Inferred relationship Some
    familliær amyloid polyneuropati, type V Is a Ocular amyloid deposit false Inferred relationship Some
    familliær amyloid polyneuropati, type V Finding site Nerve structure false Inferred relationship Some 1
    familliær amyloid polyneuropati, type V Associated morphology Amyloid deposition false Inferred relationship Some 1
    familliær amyloid polyneuropati, type V Finding site Structure of substantia propria of cornea false Inferred relationship Some 1
    familliær amyloid polyneuropati, type V Finding site Chromosome structure false Inferred relationship Some 2
    familliær amyloid polyneuropati, type V Is a Corneal stromal degeneration (disorder) false Inferred relationship Some
    familliær amyloid polyneuropati, type V Associated morphology Amyloid deposition false Inferred relationship Some 2
    familliær amyloid polyneuropati, type V Is a Hereditary amyloidosis (disorder) false Inferred relationship Some
    familliær amyloid polyneuropati, type V Is a Connective tissue hereditary disorder false Inferred relationship Some
    familliær amyloid polyneuropati, type V Is a Hereditary disorder of the visual system false Inferred relationship Some
    familliær amyloid polyneuropati, type V Is a Autosomal dominant hereditary disorder false Inferred relationship Some
    familliær amyloid polyneuropati, type V Finding site Structure of substantia propria of cornea false Inferred relationship Some 2
    familliær amyloid polyneuropati, type V Is a Hereditary disorder of nervous system false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    dystrophia corneae latticis type 2 Is a False familliær amyloid polyneuropati, type V Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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