Diagnosis Code: G11.8

Short Description: Other hereditary ataxias

Long Description: Other hereditary ataxias

The code G11.8 is VALID for claim submission

Code Classification:

• Diseases of the nervous system (G00–G99)
  • Systemic atrophies primarily affecting the central nervous system (G10-G14)
    • Hereditary ataxia (G11)
      • G11.8 Other hereditary ataxias

Code Version: 2022 ICD-10-CM

Synonyms

• 4H leukodystrophy
• Abnormal saccadic eye movement
• Acute hepatic failure
• Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome
• Arts syndrome
• Ataxia pancytopenia syndrome
• Ataxia, photosensitivity, short stature syndrome
• Autosomal dominant cerebellar ataxia type 2
• Autosomal recessive cerebellar ataxia Beauce type
• Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency
• Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome
• Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
• Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
• Autosomal recessive cerebelloparenchymal disorder type 3
• Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome
• Bailey-Cushing syndrome
• CAMOS syndrome
• Cerebellar ataxia Cayman type
• Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
• CLCN2-related leukoencephalopathy
• Congenital atrophy of optic nerve
• Congenital cerebellar ataxia due to RNU12 mutation
• Congenital non-progressive ataxia
• Episodic ataxia
• Episodic ataxia
• Episodic ataxia type 1
• Episodic ataxia type 2
• Episodic ataxia type 3
• Episodic ataxia type 4
• Episodic ataxia type 5
• Episodic ataxia type 6
• Episodic ataxia with slurred speech
• Finding of intelligibility of articulation
• Hereditary cerebellar atrophy
• Hereditary cerebellar atrophy
• Intellectual disability, hyperkinetic movement, truncal ataxia syndrome
• Jervis' syndrome
• Late tooth eruption
• Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome
• Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome
• Neuhauser Eichner Opitz syndrome
• Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome
• Progressive sensory ataxia of Charolais
• Recessive mitochondrial ataxia syndrome
• Richards-Rundle syndrome
• Sanger-Brown cerebellar ataxia
• Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome
• Slurred speech
• Spinocerebellar ataxia dysmorphism syndrome
• Spinocerebellar ataxia type 1
• Spinocerebellar ataxia type 10
• Spinocerebellar ataxia type 11
• Spinocerebellar ataxia type 12
• Spinocerebellar ataxia type 13
• Spinocerebellar ataxia type 14
• Spinocerebellar ataxia type 15/16
• Spinocerebellar ataxia type 17
• Spinocerebellar ataxia type 18
• Spinocerebellar ataxia type 19
• Spinocerebellar ataxia type 2
• Spinocerebellar ataxia type 20
• Spinocerebellar ataxia type 21
• Spinocerebellar ataxia type 23
• Spinocerebellar ataxia type 25
• Spinocerebellar ataxia type 26
• Spinocerebellar ataxia type 27
• Spinocerebellar ataxia type 28
• Spinocerebellar ataxia type 29
• Spinocerebellar ataxia type 30
• Spinocerebellar ataxia type 31
• Spinocerebellar ataxia type 32
• Spinocerebellar ataxia type 34
• Spinocerebellar ataxia type 35
• Spinocerebellar ataxia type 36
• Spinocerebellar ataxia type 37
• Spinocerebellar ataxia type 38
• Spinocerebellar ataxia type 4
• Spinocerebellar ataxia type 40
• Spinocerebellar ataxia type 41
• Spinocerebellar ataxia type 42
• Spinocerebellar ataxia type 43
• Spinocerebellar ataxia type 5
• Spinocerebellar ataxia type 6
• Spinocerebellar ataxia type 7
• Spinocerebellar ataxia type 8
• Spinocerebellar ataxia with axonal neuropathy type 1
• Third cranial nerve finding
• Truncal ataxia
• Truncal ataxia
• Unintelligible articulation

Crosswalk Information

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This page was last updated on: 10/1/2023

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