Alphabetic Index · main term

Ataxia, ataxy, ataxic

FY2027Index: At /Alphabetic Index

At the main termR27.0

Ataxia, ataxy, ataxic is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists R27.0 for the term on its own. It has 56 subterms and 49 code entries. First-level subterms include acute, autosomal recessive Friedreich, brain, cerebellar, cerebral, congenital nonprogressive, family, familial, following and more. Confirm any code you find here in the Tabular List before you report it.

Subterms 56

acuteR27.8
autosomal recessive FriedreichG11.11
brain (hereditary)G11.9
cerebellar (hereditary)G11.9
- with defective DNA repairG11.3
- alcoholicG31.2
- early-onsetG11.10
- with
  - essential tremorG11.19
  - myoclonus [Hunt's ataxia]G11.19
  - retained tendon reflexesG11.19
- in
  - alcoholismG31.2
  - myxedemaE03.9[G13.2]
  - neoplastic disease see also NeoplasmD49.9[G32.81]
  - specified disease NECG32.81
- late-onset (Marie's)G11.2
cerebral (hereditary)G11.9
congenital nonprogressiveG11.0
family, familial see Ataxia, hereditary
following
- cerebrovascular diseaseI69.993
  - cerebral infarctionI69.393
  - intracerebral hemorrhageI69.193
  - nontraumatic intracranial hemorrhage NECI69.293
  - specified disease NECI69.893
  - subarachnoid hemorrhageI69.093
Friedreich's (heredofamilial) (cerebellar) (spinal) (with retained reflexes)G11.11
gaitR26.0
- hystericalF44.4
generalR27.8
glutenM35.9[G32.81]
- with celiac diseaseK90.0[G32.81]
hereditaryG11.9
- with neuropathyG60.2
- cerebellar see Ataxia, cerebellar
- spasticG11.4
- specified NECG11.8
- spinal (Friedreich's)G11.11
heredofamilial see Ataxia, hereditary
Hunt'sG11.19
hystericalF44.4
locomotor (progressive) (syphilitic) (partial) (spastic)A52.11
- diabetic see Diabetes, ataxia
Marie's (cerebellar) (heredofamilial) (late- onset)G11.2
nonorganic originF44.4
nonprogressive, congenitalG11.0
psychogenicF44.4
Roussy-LévyG60.0
Sanger-Brown's (hereditary)G11.2
spastic hereditaryG11.4
spinal
- hereditary (Friedreich's)G11.11
- progressive (syphilitic)A52.11
spinocerebellar, X-linked recessiveG11.19
telangiectasia (Louis-Bar)G11.3