Rambaud Gallian syndrome   724002003

SNOMED CT code


SNOMED code724002003
nameRambaud Gallian syndrome
statusactive
date introduced2017-07-31
fully specified name(s)Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder)
synonyms
  • Rambaud Gallian syndrome
  • Rambaud Gallian Touchard syndrome
  • Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome
  • Retinal ischaemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome
attributes - group2
Finding siteRetinal structure   5665001
attributes - group4
Associated morphologyHyaline degeneration   19010006
Finding siteStructure of small blood vessel (organ)   27915009
attributes - group5
Associated morphologyPathologic calcification   18115005
Finding siteCerebral structure   83678007
parents
  • Hereditary degenerative disease of central nervous system   106018006
  • Cerebral calcification   17944005
  • Retinal ischemia   26468004
  • Vascular degeneration   280871000
  • Cardiovascular system hereditary disorder   363005004
  • Hereditary disorder of the visual system   363343008
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Degenerative disease of the central nervous system   80690008
          Hereditary degenerative disease of central nervous system   106018006
            Rambaud Gallian syndrome   724002003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Neurological lesion   299735001
      Lesion of brain   301766008
        Cerebral calcification   17944005
          Rambaud Gallian syndrome   724002003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Globe finding   246915008
        Retina finding   399858007
          Retinal disorder   29555009
            Retinal ischemia   26468004
              Rambaud Gallian syndrome   724002003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Vascular degeneration   280871000
          Rambaud Gallian syndrome   724002003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Disorder of cardiovascular system   49601007
        Cardiovascular system hereditary disorder   363005004
          Rambaud Gallian syndrome   724002003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Rambaud Gallian syndrome   724002003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Rambaud Gallian syndrome   724002003

ancestors
sorted most to least specific
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