Autosomal dominant neovascular inflammatory vitreoretinopathy   770791000

SNOMED CT code


SNOMED code770791000
nameAutosomal dominant neovascular inflammatory vitreoretinopathy
statusactive
date introduced2019-01-31
fully specified name(s)Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder)
synonymsAutosomal dominant neovascular inflammatory vitreoretinopathy
attributes - group1
Associated morphologyAtrophy   13331008
Finding siteVitreous body structure   47538007
attributes - group3
Clinical courseProgressive   255314001
attributes - group2
Associated morphologyAtrophy   13331008
Finding sitePeripheral retina   264141008
parents
  • Autosomal dominant hereditary disorder   11164009
  • Chronic disease of ocular adnexa   128296004
  • Vitreoretinal degeneration   247182006
  • Connective tissue hereditary disorder   363045008
  • Hereditary disorder of the visual system   363343008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Autosomal dominant neovascular inflammatory vitreoretinopathy   770791000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chronic disease   27624003
        Chronic disease of ocular adnexa   128296004
          Autosomal dominant neovascular inflammatory vitreoretinopathy   770791000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of connective tissue   105969002
        Disorder of vitreous body   76682005
          Vitreous degeneration   60189009
            Vitreoretinal degeneration   247182006
              Autosomal dominant neovascular inflammatory vitreoretinopathy   770791000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of connective tissue   105969002
        Connective tissue hereditary disorder   363045008
          Autosomal dominant neovascular inflammatory vitreoretinopathy   770791000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Autosomal dominant neovascular inflammatory vitreoretinopathy   770791000

ancestors
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