Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT code


SNOMED code237612000
namePhotomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
statusactive
date introduced2002-01-31
fully specified name(s)Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (disorder)
synonyms
  • Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
  • Herrmann syndrome
attributes - group2
Finding siteKidney structure   64033007
attributes - group3
Finding siteCerebrum   83678007
attributes - group4
Finding siteVestibulocochlear nerve structure   8598002
attributes - group5
Finding siteAuditory structure   91159003
attributes - group6
InterpretsHearing   47078008
attributes - group7
Associated withGenetic disease   782964007
attributes - group1
Finding siteEndocrine pancreatic structure   78696007
parents
  • Metabolic renal disease   106000008
  • Autosomal dominant hereditary disorder   11164009
  • Disorder of endocrine pancreas   17346000
  • Auditory system hereditary disorder   362991006
  • Digestive system hereditary disorder   363080007
  • Hereditary disorder of endocrine system   363104002
  • Hereditary disorder of nervous system   363235000
  • Hereditary nephropathy   367591000119105
  • Diabetes mellitus associated with genetic syndrome   5969009
  • Neural hearing loss   73371001
  • Disorder of brain   81308009
  • Central nervous system complication   87536007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic renal disease   106000008
          Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Finding of pancreas   300357002
        Disorder of pancreas   3855007
          Disorder of endocrine pancreas   17346000
            Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Ear and auditory finding   118236001
      Disorder of auditory system   362966006
        Auditory system hereditary disorder   362991006
          Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Disorder of digestive system   53619000
        Digestive system hereditary disorder   363080007
          Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Hereditary disorder of endocrine system   363104002
            Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of nervous system   118940003
          Hereditary disorder of nervous system   363235000
            Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Kidney finding   249578005
          Kidney disease   90708001
            Hereditary nephropathy   367591000119105
              Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Diabetes mellitus   73211009
            Secondary diabetes mellitus   8801005
              Diabetes mellitus associated with genetic syndrome   5969009
                Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of head and neck region   118254002
      Disorder of acoustic nerve   77949003
        Neural hearing loss   73371001
          Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Disorder of brain   81308009
          Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Disorder of the central nervous system   23853001
        Central nervous system complication   87536007
          Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction   237612000

ancestors
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