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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
    2574191011 Meretoja syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    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 Only initial character 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 Only initial character 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
    2580143011 Familial amyloid polyneuropathy type V en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2580144017 Finland type amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2580145016 Finnish type amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2580146015 Meretoja type amyloidosis en Synonym (core metadata concept) Active Only initial character 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
    351931000077111 syndrome de Meretoja fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    351931000077111 syndrome de Meretoja fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    syndrome de Meretoja Is a Corneal deposit (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Is a Chromosomal disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Is a Systemic amyloidosis false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Is a Disorder of soft tissue of head (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Is a Lesion of soft tissue (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Is a Neuropathy false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Is a Disorder of connective tissue false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Finding site Structure of substantia propria of cornea false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Meretoja Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Meretoja Finding site Nerve structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Meretoja Is a Corneal stroma finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Is a Ocular amyloid deposit false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Finding site Nerve structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Meretoja Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Meretoja Finding site Structure of substantia propria of cornea false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Meretoja Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Meretoja Is a Corneal stromal degeneration (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Meretoja Is a Hereditary amyloidosis (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Is a Hereditary disorder of the visual system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Meretoja Finding site Structure of substantia propria of cornea false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Meretoja Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Lattice corneal dystrophy Type II Is a False syndrome de Meretoja Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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