Autosomal dominant vitreoretinochoroidopathy   711162004

SNOMED CT code


SNOMED code711162004
nameAutosomal dominant vitreoretinochoroidopathy
statusactive
date introduced2015-07-31
fully specified name(s)Autosomal dominant vitreoretinochoroidopathy (disorder)
synonyms
  • Autosomal dominant vitreoretinochoroidopathy
  • Vitreoretinochoroidopathy with microcornea, glaucoma and cataract
  • Autosomal dominant vitreoretinochoroidopathy with nanophthalmos
attributes - group1
Associated morphologyDystrophy   4720007
Finding siteRetinal structure   5665001
parents
  • Autosomal dominant hereditary disorder   11164009
  • Hereditary retinal dystrophy   41799005
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 vitreoretinochoroidopathy   711162004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Hereditary retinal dystrophy   41799005
            Autosomal dominant vitreoretinochoroidopathy   711162004

ancestors
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