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419398009: Meretoja syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    2574191011 Meretoja syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    2577530013 Meretoja syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
    2580142018 Amyloid cranial neuropathy with lattice corneal dystrophy en Synonym Active Entire term case insensitive SNOMED CT core module
    2580143011 Familial amyloid polyneuropathy type V en Synonym Inactive Only initial character case insensitive SNOMED CT core module
    2580144017 Finland type amyloidosis en Synonym Inactive Entire term case sensitive SNOMED CT core module
    2580145016 Finnish type amyloidosis en Synonym Inactive Entire term case sensitive SNOMED CT core module
    2580146015 Meretoja type amyloidosis en Synonym Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

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

    This concept is not in any reference sets

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