G11.8
BillableOther hereditary ataxias
Other hereditary ataxias
Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- cerebral palsy (G80.-)
- hereditary and idiopathic neuropathy (G60.-)
- metabolic disorders (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Delayed dentition5639000
- Delayed eruption of tooth5639000
- Delayed tooth eruption5639000
- Late tooth eruption5639000
- Sanger-Brown cerebellar ataxia37960002
- Early familial cerebellar degeneration syndrome45897005
- Jervis' syndrome45897005
- Bailey-Cushing syndrome60146005
- Cerebellar midline syndrome60146005
- Oculomotor nerve finding106153001
- Third cranial nerve finding106153001
- ALF - Acute liver failure197270009
- Acute hepatic failure197270009
- Acute liver failure197270009
- Slow to talk229721007
- Speech delay229721007
- Abnormal saccadic eye movement246767003
- Dysmetric ataxia246767003
- Truncal ataxia250067008
- Congenital non-progressive ataxia278509004
- Finding of intelligibility of articulation289193001
- Observation of clarity of speech289193001
- Observation of intelligibility of articulation289193001
- Observation of intelligibility of speech289193001
- Unintelligible articulation289194007
- Unintelligible speech289194007
- Clipped speech289195008
- Scamping speech289195008
- Slurred speech289195008
- Slurring289195008
- Episodic ataxia type 2420932006
- Episodic ataxia type 2 (EA2)420932006
- Episodic ataxia type 1421182009
- Episodic ataxia type 1 (EA1)421182009
- Episodic ataxia421455009
- Arts syndrome702441001
- Fatal X-linked ataxia with deafness and loss of vision702441001
- Lethal ataxia-deafness-optic atrophy702441001
- Asidan ataxia711158005
- Costa de Morte ataxia711158005
- Spinocerebellar ataxia 36711158005
- Spinocerebellar ataxia type 36711158005
- Autosomal recessive cerebelloparenchymal disorder type 3715369006
- Cerebelloparenchymal disorder III715369006
- SCAR2 (spinocerebellar ataxia autosomal recessive 2)715369006
- Richards-Rundle syndrome715415005
- Ataxia with pigmentary retinopathy715726000
- Cerebellar syndrome pigmentary maculopathy715726000
- Spinocerebellar ataxia type 7715726000
- Spinocerebellar ataxia type 1715748006
- Spinocerebellar ataxia type 2715751004
- Spinocerebellar ataxia type 6715752006
- Spinocerebellar ataxia type 8715753001
- Spinocerebellar ataxia type 10715754007
- Spinocerebellar ataxia type 4715755008
- Spinocerebellar ataxia type 28715824008
- Congenital nonprogressive spinocerebellar ataxia715825009
- Spinocerebellar ataxia type 29715825009
- Spinocerebellar ataxia type 31715826005
- Spinocerebellar ataxia type 15/16716724006
- Cayman ataxia717332007
- Cerebellar ataxia Cayman type717332007
- Episodic ataxia type 6718753002
- Episodic ataxia type 4718754008
- Periodic vestibulocerebellar ataxia718754008
- Episodic ataxia and vertigo with tinnitus and myokymia syndrome718755009
- Episodic ataxia type 3718755009
- Episodic ataxia type 5718756005
- Spinocerebellar ataxia type 26718769009
- Spinocerebellar ataxia type 25718770005
- Spinocerebellar ataxia type 20718771009
- Spinocerebellar ataxia type 23718772002
- Spinocerebellar ataxia type 21718774001
- Spinocerebellar ataxia type 11719207000
- Spinocerebellar ataxia type 12719208005
- Spinocerebellar ataxia type 13719209002
- Spinocerebellar ataxia type 14719210007
- Huntington disease-like 4719249005
- Spinocerebellar ataxia type 17719249005
- Spinocerebellar ataxia type 18719250005
- Spinocerebellar ataxia type 19719251009
- Spinocerebellar ataxia type 27719252002
- Spinocerebellar ataxia type 30719253007
- Spinocerebellar ataxia type 32719254001
- Erythrokeratodermia with ataxia719255000
- Spinocerebellar ataxia and erythrokeratodermia719255000
- Spinocerebellar ataxia type 34719255000
- Spinocerebellar ataxia type 35719300001
- Spinocerebellar ataxia type 37719301002
- Spinocerebellar ataxia with altered vertical eye movement719301002
- Spinocerebellar ataxia type 5719302009
- Congenital atrophy of optic nerve722990003
- Congenital optic atrophy722990003
- ARCA1 - autosomal recessive cerebellar ataxia type 1725433003
- Autosomal recessive cerebellar ataxia Beauce type725433003
- CAMOS (cerebellar ataxia, mental retardation, optic atrophy, skin abnormalities) syndrome726031001
- CAMOS syndrome726031001
- Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome726031001
- SCAR5 - spinocerebellar ataxia autosomal recessive 5726031001
- Spinocerebellar ataxia dysmorphism syndrome733033001
- Spinocerebellar ataxia type 40734020000
- Spinocerebellar ataxia type 38734021001
- Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome763312008
- Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome763344007
- Poretti Boltshauser syndrome763344007
- Ataxia, delayed dentition, hypomyelination syndrome764095005
- Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome764095005
- Spinocerebellar ataxia with axonal neuropathy type 1765091006
- Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome766814006
- Ataxia pancytopenia syndrome768556005
- Myelocerebellar disorder768556005
- CLCN2 (chloride voltage-gated channel 2) related leucoencephalopathy768663003
- CLCN2 (chloride voltage-gated channel 2) related leukoencephalopathy768663003
- CLCN2-related leucoencephalopathy768663003
- CLCN2-related leukoencephalopathy768663003
- Leucoencephalopathy with ataxia768663003
- Leucoencephalopathy with mild cerebellar ataxia and white matter oedema768663003
- Leukoencephalopathy with ataxia768663003
- Leukoencephalopathy with mild cerebellar ataxia and white matter edema768663003
- Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency770898002
- Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency770898002
- Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency770898002
- Autosomal recessive spinocerebellar ataxia type 12770898002
- Episodic ataxia type 8773495009
- Episodic ataxia with slurred speech773495009
- Ataxia, photosensitivity, short stature syndrome773769008
- Fenton Wilkinson Toselano syndrome773769008
- MIRAS - mitochondrial recessive ataxia syndrome782696001
- Recessive mitochondrial ataxia syndrome782696001
- Intellectual disability, hyperkinetic movement, truncal ataxia syndrome787174003
- Non-progressive cerebellar ataxia1119354003
- Progressive truncal ataxia1119356001
- Autosomal dominant cerebellar ataxia type 21156796002
- Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation1177169004
- Congenital cerebellar ataxia due to RNU12 mutation1177169004
- Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome1187643003
- Autosomal recessive spinocerebellar ataxia type 211187643003
- Autosomal recessive spinocerebellar ataxia type 31204415006
- Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome1204415006
- Autosomal recessive spinocerebellar ataxia, blindness, hearing loss syndrome1204415006
- SCAR3 - spinocerebellar ataxia autosomal recessive type 31204415006
- Neuhauser Eichner Opitz syndrome1208339007
- Recurrent encephalopathy of childhood1208339007
- Spinocerebellar ataxia type 411208512000
- Spinocerebellar ataxia type 421208513005
- Spinocerebellar ataxia type 431208516002
- Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome1208727002
- 4H leucodystrophy1208933000
- 4H leukodystrophy1208933000
- POLR-related leucodystrophy1208933000
- POLR-related leukodystrophy1208933000
- Lichtenstein Knorr syndrome1237413006
- Progressive autosomal recessive ataxia, deafness syndrome1237413006
- Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome1237413006
- SCAR19 - spinocerebellar ataxia, autosomal recessive 191237413006
- Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome1237514002
- Mitochondrial myopathy, cerebellar atrophy, pigmentary retinopathy syndrome1237514002
- Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency1237625002
- Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency1237625002
- SCAR17 - spinocerebellar ataxia autosomal recessive type 171237625002
- DHX30-related neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome1363573005
- DHX30-related neurodevelopmental disorder1363573005
- Neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome1363573005
- Hereditary cerebellar atrophy431641000124107
Frequently Asked Questions
What is ICD-10 code G11.8?
ICD-10-CM code G11.8 represents "Other hereditary ataxias". It is a billable/specific code that can be used on a claim.
Is G11.8 a billable code?
Yes, G11.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G11.8 in?
G11.8 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G11.8 map to?
G11.8 maps to 90 SNOMED CT concepts: 1208933000, 197270009, 725433003, 246767003, 1187643003, and 85 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G11.8?
G11.8 is linked to 1 UMLS Concept Unique Identifier: C0477348. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.