G60.2
BillableNeuropathy in association with hereditary ataxia
Neuropathy in association with hereditary ataxia
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(5)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(46)
SNOMED CT
- VOR - vestibuloocular reflex90906005
- Vestibulo-ocular reflex finding90906005
- Vestibuloocular reflex90906005
- Neuropathy in association with hereditary ataxia193165008
- Chronic neuropathy with no known cause or association230655004
- Idiopathic chronic neuropathy230655004
- Chronic idiopathic ataxic neuropathy230658002
- Vestibulo-ocular reflex absent299818006
- Sensory ataxia445458007
- SANDO (sensory ataxic neuropathy dysarthria ophthalmoparesis) syndrome717266001
- Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome717266001
- Acquired dysarthria719316004
- Chronic bilateral vestibulopathy722952009
- PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract) syndrome723452007
- PHARC syndrome723452007
- Peripheral neuropathy Fiskerstrand type723452007
- Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome723452007
- Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome1222655009
- CABV (cerebellar ataxia, bilateral vestibulopathy) syndrome1236804009
- CANVAS - cerebellar ataxia, neuropathy, vestibular areflexia syndrome1236804009
- Cerebellar ataxia with bilateral vestibulopathy syndrome1236804009
- Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome1236804009
UMLS
Clinical Terms
- Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
- Vestibuloocular reflex
- PHARC syndrome
- Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome
- Acquired dysarthria
- Neuropathy in association with hereditary ataxia (disorder)
- Vestibulo-ocular reflex finding
- Vestibulo-ocular reflex absent
- VOR - vestibuloocular reflex
- PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract) syndrome
- CANVAS - cerebellar ataxia, neuropathy, vestibular areflexia syndrome
- CABV (cerebellar ataxia, bilateral vestibulopathy) syndrome
- Chronic idiopathic ataxic neuropathy
- Chronic bilateral vestibulopathy
- Peripheral neuropathy Fiskerstrand type
- Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome
- SANDO (sensory ataxic neuropathy dysarthria ophthalmoparesis) syndrome
- Cerebellar ataxia with bilateral vestibulopathy syndrome
- Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
- Chronic neuropathy with no known cause or association
- Sensory ataxia
- Idiopathic chronic neuropathy
Frequently Asked Questions
What is the ICD-10 code for neuropathy in association with hereditary ataxia?
The ICD-10-CM code for neuropathy in association with hereditary ataxia is G60.2. The full clinical description is "Neuropathy in association with hereditary ataxia". G60.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G60.2 mean?
ICD-10-CM code G60.2 represents “Neuropathy in association with hereditary ataxia”. 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 G60.2 a billable code?
Yes, G60.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G60.2 in?
G60.2 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G60.2?
G60.2 has Excludes1 notes indicating codes that cannot be used together with it, including: neuralgia NOS (M79.2); neuritis NOS (M79.2); peripheral neuritis in pregnancy (O26.82-); and 1 more.
What SNOMED CT codes does G60.2 map to?
G60.2 maps to 12 SNOMED CT concepts: 719316004, 1236804009, 722952009, 230658002, 230655004, and 7 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G60.2?
G60.2 is linked to 1 UMLS Concept Unique Identifier: C0451669. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G60.2 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like neuropathy in association with hereditary ataxia 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 G60.2?
G60.2 maps to the ICD-11 code: 8A03.15 (Ataxia due to mitochondrial mutations).
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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.