G11.11
Friedreich ataxia
HCC risk adjustment mapping
CMS-HCC V28
Friedreich and Other Hereditary Ataxias; Huntington Disease
CMS-HCC ESRD V24
Spinal Cord Disorders/Injuries
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
Autosomal recessive Friedreich ataxia Friedreich ataxia with retained reflexes
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)
Official Guidelines for G11.11
FY 2026 ›Find G11.11 in the alphabetic index
13 index paths lead to this code
- Ataxia, ataxy, ataxic › autosomal recessive Friedreich
- Ataxia, ataxy, ataxic › Friedreich's
- Friedreich's › ataxia
- Friedreich's › combined systemic disease
- Friedreich's › sclerosis
- Sclerosis, sclerotic › Friedreich's
- Ataxia, ataxy, ataxic › hereditary › spinal
- Ataxia, ataxy, ataxic › spinal › hereditary
- Cardiomyopathy › due to › Friedreich's ataxia
- Disease, diseased › Friedreich's › combined systemic or ataxia
- Myocardiopathy › in › Friedreich's ataxia
- Sclerosis, sclerotic › hereditary › spinal
- Sclerosis, sclerotic › spinal › hereditary