Myelocerebellar disorder
Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome
Episodic ataxia type 1
Autosomal recessive cerebellar ataxia Beauce type
4H leucodystrophy
Autosomal recessive spinocerebellar ataxia type 21
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
Congenital cerebellar ataxia due to RNU12 mutation
Costa de Morte ataxia
Episodic ataxia type 2
Ataxia pancytopenia syndrome
Observation of intelligibility of articulation
Spinocerebellar ataxia type 13
Cerebellar midline syndrome
Cerebelloparenchymal disorder III
Lethal ataxia-deafness-optic atrophy
SCAR2 (spinocerebellar ataxia autosomal recessive 2)
Asidan ataxia
Ataxia, delayed dentition, hypomyelination syndrome
Spinocerebellar ataxia type 6
Congenital atrophy of optic nerve
Fenton Wilkinson Toselano syndrome
Mitochondrial myopathy, cerebellar atrophy, pigmentary retinopathy syndrome
Spinocerebellar ataxia and erythrokeratodermia
Speech delay
Ataxia with pigmentary retinopathy
Sanger-Brown cerebellar ataxia
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome
Bailey-Cushing syndrome
Spinocerebellar ataxia type 4
Delayed dentition
Episodic ataxia type 3
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome
Clipped speech
Spinocerebellar ataxia type 23
Recurrent encephalopathy of childhood
Spinocerebellar ataxia with axonal neuropathy type 1
Spinocerebellar ataxia type 42
Jervis' syndrome
Hereditary cerebellar atrophy
Episodic ataxia type 1 (EA1)
SCAR19 - spinocerebellar ataxia, autosomal recessive 19
Poretti Boltshauser syndrome
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
Richards-Rundle syndrome
Progressive truncal ataxia
CAMOS (cerebellar ataxia, mental retardation, optic atrophy, skin abnormalities) syndrome
Spinocerebellar ataxia type 40
Dysmetric ataxia
Slurred speech
Spinocerebellar ataxia dysmorphism syndrome
Autosomal recessive spinocerebellar ataxia type 12
POLR-related leucodystrophy
Huntington disease-like 4
Acute hepatic failure
Spinocerebellar ataxia type 20
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Early familial cerebellar degeneration syndrome
Delayed eruption of tooth
Fatal X-linked ataxia with deafness and loss of vision
Spinocerebellar ataxia type 7
Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
POLR-related leukodystrophy
Spinocerebellar ataxia with altered vertical eye movement
ARCA1 - autosomal recessive cerebellar ataxia type 1
Congenital non-progressive ataxia
Spinocerebellar ataxia type 21
Spinocerebellar ataxia type 31
Spinocerebellar ataxia type 1
Erythrokeratodermia with ataxia
Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome
Cayman ataxia
DHX30-related neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome
Spinocerebellar ataxia type 19
Spinocerebellar ataxia type 15/16
Acute liver failure
Spinocerebellar ataxia type 41
Autosomal recessive cerebelloparenchymal disorder type 3
Intellectual disability, hyperkinetic movement, truncal ataxia syndrome
Spinocerebellar ataxia type 8
Progressive autosomal recessive ataxia, deafness syndrome
Arts syndrome
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome
Recessive mitochondrial ataxia syndrome
Autosomal recessive spinocerebellar ataxia, blindness, hearing loss syndrome
Ataxia, photosensitivity, short stature syndrome
Finding of intelligibility of articulation
SCAR17 - spinocerebellar ataxia autosomal recessive type 17
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome
Spinocerebellar ataxia type 30
Autosomal recessive spinocerebellar ataxia type 3
Non-progressive cerebellar ataxia
Observation of clarity of speech
DHX30-related neurodevelopmental disorder
Oculomotor nerve finding
Spinocerebellar ataxia type 25
Spinocerebellar ataxia type 5
Spinocerebellar ataxia type 2
Autosomal dominant cerebellar ataxia type 2
Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome
Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency
CLCN2-related leukoencephalopathy
Leukoencephalopathy with ataxia
MIRAS - mitochondrial recessive ataxia syndrome
Slurring
Spinocerebellar ataxia type 12
Episodic ataxia type 4
Leucoencephalopathy with ataxia
Spinocerebellar ataxia type 27
SCAR5 - spinocerebellar ataxia autosomal recessive 5
Spinocerebellar ataxia type 38
Episodic ataxia type 6
Spinocerebellar ataxia type 34
Leucoencephalopathy with mild cerebellar ataxia and white matter oedema
Congenital optic atrophy
Lichtenstein Knorr syndrome
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency
Spinocerebellar ataxia type 26
Truncal ataxia
Delayed tooth eruption
Episodic ataxia type 8
Spinocerebellar ataxia 36
Episodic ataxia
Episodic ataxia with slurred speech
Scamping speech
Episodic ataxia type 5
Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency
Spinocerebellar ataxia type 14
CLCN2-related leucoencephalopathy
Spinocerebellar ataxia type 37
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
Unintelligible speech
Cerebellar ataxia Cayman type
Neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome
CLCN2 (chloride voltage-gated channel 2) related leucoencephalopathy
Spinocerebellar ataxia type 36
CAMOS syndrome
Spinocerebellar ataxia type 11
4H leukodystrophy
Late tooth eruption
Spinocerebellar ataxia type 35
Unintelligible articulation
Spinocerebellar ataxia type 32
Abnormal saccadic eye movement
Episodic ataxia type 2 (EA2)
Observation of intelligibility of speech
Spinocerebellar ataxia type 17
SCAR3 - spinocerebellar ataxia autosomal recessive type 3
CLCN2 (chloride voltage-gated channel 2) related leukoencephalopathy
Third cranial nerve finding
Cerebellar syndrome pigmentary maculopathy
Spinocerebellar ataxia type 29
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome
Neuhauser Eichner Opitz syndrome
Congenital nonprogressive spinocerebellar ataxia
Episodic ataxia and vertigo with tinnitus and myokymia syndrome
Slow to talk
Spinocerebellar ataxia type 10
Spinocerebellar ataxia type 28
Periodic vestibulocerebellar ataxia
Spinocerebellar ataxia type 43
Spinocerebellar ataxia type 18
ALF - Acute liver failure

Frequently Asked Questions

What is the ICD-10 code for other hereditary ataxias?

The ICD-10-CM code for other hereditary ataxias is G11.8. The full clinical description is "Other hereditary ataxias". G11.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code G11.8 mean?

ICD-10-CM code G11.8 represents “Other hereditary ataxias”. It is classified under Chapter 6: Diseases of the Nervous System and 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.

How does G11.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other hereditary ataxias affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of G11.8?

G11.8 maps to the ICD-11 code: 8A03.Z (Ataxic disorders, unspecified).

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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.