ICD-10-CM Alphabetic Index to Diseases and Injuries
Ataxia, ataxy, ataxic
Default code: R27.0. Follow the subterms below to reach a more specific code.ICD-10 code for Ataxia — guide and common questions →
- acute R27.8
- autosomal recessive Friedreich G11.11
- brain (hereditary) G11.9
- cerebellar (hereditary) G11.9
- with defective DNA repair G11.3
- alcoholic G31.2
- early-onset G11.10
- with
- essential tremor G11.19
- myoclonus [Hunt's ataxia] G11.19
- retained tendon reflexes G11.19
- in
- alcoholism G31.2
- myxedema E03.9
- neoplastic disease D49.9 — see also Neoplasm
- specified disease NEC G32.81
- late-onset (Marie's) G11.2
- cerebral (hereditary) G11.9
- congenital nonprogressive G11.0
- family, familial — see Ataxia, hereditary
- following
- cerebrovascular disease I69.993
- cerebral infarction I69.393
- intracerebral hemorrhage I69.193
- nontraumatic intracranial hemorrhage NEC I69.293
- specified disease NEC I69.893
- subarachnoid hemorrhage I69.093
- Friedreich's (heredofamilial) (cerebellar) (spinal) (with retained reflexes) G11.11
- gait R26.0
- hysterical F44.4
- general R27.8
- gluten M35.9
- with celiac disease K90.0
- hereditary G11.9
- with neuropathy G60.2
- cerebellar — see Ataxia, cerebellar
- spastic G11.4
- specified NEC G11.8
- spinal (Friedreich's) G11.11
- heredofamilial — see Ataxia, hereditary
- Hunt's G11.19
- hysterical F44.4
- locomotor (progressive) (syphilitic) (partial) (spastic) A52.11
- diabetic — see Diabetes, ataxia
- Marie's (cerebellar) (heredofamilial) (late- onset) G11.2
- nonorganic origin F44.4
- nonprogressive, congenital G11.0
- psychogenic F44.4
- Roussy-Lévy G60.0
- Sanger-Brown's (hereditary) G11.2
- spastic hereditary G11.4
- spinal
- hereditary (Friedreich's) G11.11
- progressive (syphilitic) A52.11
- spinocerebellar, X-linked recessive G11.19
- telangiectasia (Louis-Bar) G11.3