ICD-10-CM Code G11: Hereditary ataxia and Related Diagnosis Codes.

The ICD-10-CM (the International Classification of Diseases, Tenth Revision, Clinical Modification) is a standardized coding system used when classifying diseases and medical conditions. Healthcare providers report these codes on Medical claims when diagnosing patient care.

Explore ICD-10-CM codes, organized by chapters based on body systems and medical conditions, as outlined in the International Classification of Diseases, Tenth Revision, Clinical Modification.

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A categorized list of ICD-10-CM codes organized by chapters based on body systems or medical conditions, according to the International Classification of Diseases, Tenth Revision, Clinical Modification.

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  • G11 - Hereditary ataxia
    • G11.0 - Congenital nonprogressive ataxia
    • G11.1 - Early-onset cerebellar ataxia
      • G11.10 - Early-onset cerebellar ataxia, unspecified
      • G11.11 - Friedreich ataxia
      • G11.19 - Other early-onset cerebellar ataxia
    • G11.2 - Late-onset cerebellar ataxia
    • G11.3 - Cerebellar ataxia with defective DNA repair
    • G11.4 - Hereditary spastic paraplegia
    • G11.5 - Hypomyelination - hypogonadotropic hypogonadism - hypodontia
    • G11.6 - Leukodystrophy with vanishing white matter disease
    • G11.8 - Other hereditary ataxias
    • G11.9 - Hereditary ataxia, unspecified
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Note: The International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) codes are developed and maintained by the Centers for Disease Control and Prevention (CDC). CDC's National Center for Health Statistics (NCHS) is responsible for the clinical modification of ICD-10 for use in the United States. The World Health Organization (WHO), which owns and publishes ICD-10, authorized NCHS to develop ICD-10-CM. All modifications to ICD-10 must conform to WHO's established ICD structure and conventions. All rights are reserved by the respective entities.