Alphabetic index · A

Ataxia, ataxy, ataxic

R27.0default code

Sub-terms

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
myxedemaE03.9G13.2
neoplastic diseasesee also NeoplasmD49.9G32.81
specified disease NECG32.81
late-onset (Marie's)G11.2
cerebral (hereditary)G11.9
congenital nonprogressiveG11.0
family, familialsee 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
glutenM35.9G32.81
with celiac diseaseK90.0G32.81
hereditaryG11.9
with neuropathyG60.2
spasticG11.4
specified NECG11.8
spinal (Friedreich's)G11.11
Hunt'sG11.19
hystericalF44.4
locomotor (progressive) (syphilitic) (partial) (spastic)A52.11
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

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