Wolfram-like syndrome   734022008

SNOMED CT code


SNOMED code734022008
nameWolfram-like syndrome
statusactive
date introduced2017-07-31
fully specified name(s)Wolfram-like syndrome (disorder)
synonymsWolfram-like syndrome
attributes - group4
Due toGenetic disease   782964007
attributes - group2
InterpretsHearing   47078008
attributes - group5
OccurrenceCongenital   255399007
Finding siteEndocrine structure   113331007
attributes - group6
OccurrenceCongenital   255399007
Finding siteEar structure   117590005
attributes - group7
OccurrenceCongenital   255399007
Associated morphologyPrimary atrophy   68616007
Finding siteOptic nerve structure   18234004
parents
  • Autosomal dominant hereditary disorder   11164009
  • Hearing loss associated with syndrome   232333009
  • Disorder of ear   25906001
  • Hereditary optic atrophy   26360005
  • Auditory system hereditary disorder   362991006
  • Hereditary disorder of endocrine system   363104002
  • Diabetes mellitus associated with genetic syndrome   5969009
  • Congenital atrophy of optic nerve   722990003
  • Central nervous system complication   87536007
  • Congenital hearing disorder   95827002
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
              Wolfram-like syndrome   734022008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Hearing finding   118230007
        Hearing disorder   128540005
          Hearing loss   15188001
            Hearing loss associated with syndrome   232333009
              Wolfram-like syndrome   734022008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of sensory organ   1279550006
        Disorder of ear   25906001
          Wolfram-like syndrome   734022008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Inherited optic neuropathy   312942003
            Hereditary optic atrophy   26360005
              Wolfram-like syndrome   734022008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Ear and auditory finding   118236001
      Disorder of auditory system   362966006
        Auditory system hereditary disorder   362991006
          Wolfram-like syndrome   734022008

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
            Wolfram-like syndrome   734022008

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
                Wolfram-like syndrome   734022008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital atrophy of optic nerve   722990003
          Wolfram-like syndrome   734022008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Disorder of the central nervous system   23853001
        Central nervous system complication   87536007
          Wolfram-like syndrome   734022008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hearing disorder   95827002
          Wolfram-like syndrome   734022008

ancestors
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