Ataxia, ataxy, ataxic

"Ataxia, ataxy, ataxic" References in the ICD-10-CM Index to Diseases and Injuries

References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term "ataxia, ataxy, ataxic"

• Ataxia, ataxy, ataxic - R27.0 Ataxia, unspecified
  • acute - R27.8 Other lack of coordination
  • autosomal recessive Friedreich - G11.11 Friedreich ataxia
  • brain (hereditary) - G11.9 Hereditary ataxia, unspecified
  • cerebellar (hereditary) - G11.9 Hereditary ataxia, unspecified
    • alcoholic - G31.2 Degeneration of nervous system due to alcohol
    • early-onset - G11.10 Early-onset cerebellar ataxia, unspecified
    • in
      • alcoholism - G31.2 Degeneration of nervous system due to alcohol
      • myxedema - E03.9 Hypothyroidism, unspecified
      • neoplastic disease - See Also: Neoplasm; - D49.9 Neoplasm of unspecified behavior of unspecified site
      • specified disease NEC - G32.81 Cerebellar ataxia in diseases classified elsewhere
    • late-onset (Marie's) - G11.2 Late-onset cerebellar ataxia
    • with
      • essential tremor - G11.19 Other early-onset cerebellar ataxia
      • myoclonus [Hunt's ataxia] - G11.19 Other early-onset cerebellar ataxia
      • retained tendon reflexes - G11.19 Other early-onset cerebellar ataxia
    • with defective DNA repair - G11.3 Cerebellar ataxia with defective DNA repair
  • cerebral (hereditary) - G11.9 Hereditary ataxia, unspecified
  • congenital nonprogressive - G11.0 Congenital nonprogressive ataxia
  • family, familial - See: Ataxia, hereditary;
  • following
    • cerebrovascular disease - I69.993 Ataxia following unspecified cerebrovascular disease
      • cerebral infarction - I69.393 Ataxia following cerebral infarction
      • intracerebral hemorrhage - I69.193 Ataxia following nontraumatic intracerebral hemorrhage
      • nontraumatic intracranial hemorrhage NEC - I69.293 Ataxia following other nontraumatic intracranial hemorrhage
      • specified disease NEC - I69.893 Ataxia following other cerebrovascular disease
      • subarachnoid hemorrhage - I69.093 Ataxia following nontraumatic subarachnoid hemorrhage
  • Friedreich's (heredofamilial) (cerebellar) (spinal) (with retained reflexes) - G11.11 Friedreich ataxia
  • gait - R26.0 Ataxic gait
    • hysterical - F44.4 Conversion disorder with motor symptom or deficit
  • general - R27.8 Other lack of coordination
  • gluten - M35.9 Systemic involvement of connective tissue, unspecified
    • with celiac disease - K90.0 Celiac disease
  • hereditary - G11.9 Hereditary ataxia, unspecified
    • cerebellar - See: Ataxia, cerebellar;
    • spastic - G11.4 Hereditary spastic paraplegia
    • specified NEC - G11.8 Other hereditary ataxias
    • spinal (Friedreich's) - G11.11 Friedreich ataxia
    • with neuropathy - G60.2 Neuropathy in association with hereditary ataxia
  • heredofamilial - See: Ataxia, hereditary;
  • Hunt's - G11.19 Other early-onset cerebellar ataxia
  • hysterical - F44.4 Conversion disorder with motor symptom or deficit
  • locomotor (progressive) (syphilitic) (partial) (spastic) - A52.11 Tabes dorsalis
    • diabetic - See: Diabetes, ataxia;
  • Marie's (cerebellar) (heredofamilial) (late- onset) - G11.2 Late-onset cerebellar ataxia
  • nonorganic origin - F44.4 Conversion disorder with motor symptom or deficit
  • nonprogressive, congenital - G11.0 Congenital nonprogressive ataxia
  • psychogenic - F44.4 Conversion disorder with motor symptom or deficit
  • Roussy-Lévy - G60.0 Hereditary motor and sensory neuropathy
  • Sanger-Brown's (hereditary) - G11.2 Late-onset cerebellar ataxia
  • spastic hereditary - G11.4 Hereditary spastic paraplegia
  • spinal
    • hereditary (Friedreich's) - G11.11 Friedreich ataxia
    • progressive (syphilitic) - A52.11 Tabes dorsalis
  • spinocerebellar, X-linked recessive - G11.19 Other early-onset cerebellar ataxia
  • telangiectasia (Louis-Bar) - G11.3 Cerebellar ataxia with defective DNA repair