Congenital hereditary endothelial dystrophy   417651000

SNOMED CT code


SNOMED code417651000
nameCongenital hereditary endothelial dystrophy
statusactive
date introduced2005-07-31
fully specified name(s)Congenital hereditary endothelial dystrophy (disorder)
synonyms
  • Congenital hereditary endothelial dystrophy
  • CHED-congenital hereditary endothelial dystrophy
attributes - group2
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteChromosome pair 20   25610001
Associated morphologyCellular AND/OR subcellular abnormality   107673000
attributes - group1
Associated morphologyDystrophy   4720007
Finding siteStructure of corneal endothelium   65431007
parents
children
  • Congenital hereditary endothelial dystrophy and perceptive deafness syndrome   720749004
  • Congenital hereditary endothelial dystrophy type 1   416633008
  • Congenital hereditary endothelial dystrophy type 2   417395001
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital hereditary endothelial dystrophy   417651000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Congenital hereditary endothelial dystrophy   417651000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Globe finding   246915008
        Anterior segment finding   418727003
          Corneal finding   246924004
            Corneal endothelium finding   246966003
              Corneal endothelial dystrophy   416960004
                Congenital hereditary endothelial dystrophy   417651000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Hereditary corneal dystrophy   77797009
            Congenital hereditary endothelial dystrophy   417651000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chromosomal disorder   409709004
        Congenital chromosomal disease   74345006
          Anomaly of chromosome pair   362984008
            Anomaly of chromosome pair 20   9839007
              Congenital hereditary endothelial dystrophy   417651000

ancestors
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