Ataxia, ataxy, ataxic - in the ICD-10-CM Index

Browse the ICD-10-CM codes with references 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

Gait: Manner or style of walking.