Hereditary Retinal Dystrophies (1522)    NLM VALUE SETS (802.2)

Name Value
NAME Hereditary Retinal Dystrophies
OID 2.16.840.1.113883.3.526.3.1463
SHORT ID HRD63
VERSION DATE 2017-01-06 00:00:00
CODE LIST
  • CODES:
    • CODE DESCRIPTION:   
      Retinal dystrophy in systemic lipidosis (disorder)
    • CODE DESCRIPTION:   
      Hyaline retinal dystrophy (disorder)
    • CODE DESCRIPTION:   
      Tapetoretinal dystrophy (disorder)
    • CODE DESCRIPTION:   
      Autosomal dominant retinitis pigmentosa (disorder)
    • CODE DESCRIPTION:   
      Autosomal recessive retinitis pigmentosa (disorder)
    • CODE DESCRIPTION:   
      Progressive rod dystrophy (disorder)
    • CODE DESCRIPTION:   
      Usher syndrome type 1 (disorder)
    • CODE DESCRIPTION:   
      Usher syndrome type 2 (disorder)
    • CODE DESCRIPTION:   
      Progressive cone dystrophy (without rod involvement) (disorder)
    • CODE DESCRIPTION:   
      Cone dystrophy (disorder)
    • CODE DESCRIPTION:   
      Rod dystrophy (disorder)
    • CODE DESCRIPTION:   
      Retinitis pigmentosa (disorder)
    • CODE DESCRIPTION:   
      Hereditary retinal dystrophy (disorder)
    • CODE DESCRIPTION:   
      Retinitis pigmentosa-deafness syndrome (disorder)
    • CODE DESCRIPTION:   
      Pigmentary retinal dystrophy (disorder)
    • CODE DESCRIPTION:   
      Vitreoretinal dystrophy (disorder)
    • CODE DESCRIPTION:   
      Progressive cone-rod dystrophy (disorder)
    • CODE DESCRIPTION:   
      Retinal dystrophy in cerebroretinal lipidosis (disorder)
    • CODE DESCRIPTION:   
      Hereditary retinal dystrophies in lipidoses (disorder)
  • CODES:
    • CODE DESCRIPTION:   
      Retinal dystrophy in systemic or cerebroretinal lipidoses
    • CODE DESCRIPTION:   
      Retinal dystrophy in other systemic disorders and syndromes
    • CODE DESCRIPTION:   
      Vitreoretinal dystrophies
    • CODE DESCRIPTION:   
      Pigmentary retinal dystrophy
    • CODE DESCRIPTION:   
      Other dystrophies primarily involving the sensory retina
    • CODE DESCRIPTION:   
      Dystrophies primarily involving the retinal pigment epithelium
    • CODE:   362.70
      CODE DESCRIPTION:   
      Hereditary retinal dystrophy, unspecified
  • CODES:
    • CODE:   H35.50
      CODE DESCRIPTION:   
      Unspecified hereditary retinal dystrophy
    • CODE:   H35.51
      CODE DESCRIPTION:   
      Vitreoretinal dystrophy
    • CODE:   H35.52
      CODE DESCRIPTION:   
      Pigmentary retinal dystrophy
    • CODE:   H35.53
      CODE DESCRIPTION:   
      Other dystrophies primarily involving the sensory retina
    • CODE:   H35.54
      CODE DESCRIPTION:   
      Dystrophies primarily involving the retinal pigment epithelium
    • CODE:   H36
      CODE DESCRIPTION:   
      Retinal disorders in diseases classified elsewhere
MEASURE LIST