Azorean disease
Cerebellar ataxia loss of muscle coordination)
Cervical neuromuscular scoliosis due to friedreich’s ataxia
Cervical scoliosis due to friedreichs ataxia
Cervicothoracic neuromuscular scoliosis due to friedreich’s ataxia
Cervicothoracic scoliosis due to friedreichs ataxia
Early onset cerebellar ataxia
Friedreich’s ataxia
Friedreichs ataxia
Josephs disease
Lumbar neuromuscular scoliosis due to friedreich’s ataxia
Lumbar scoliosis due to friedreichs ataxia
Lumbosacral neuromuscular scoliosis due to friedreich’s ataxia
Lumbosacral scoliosis due to friedreichs ataxia
Machado joseph disease
Neuromuscular scoliosis due to friedreich’s ataxia
Neuromuscular scoliosis due to friedreichs ataxia
Occipitoatlantoaxial neuromuscular scoliosis due to friedreich’s ataxia
Occipitoatlantoaxial scoliosis in friedreichs ataxia
Spinocerebellar ataxia
Thoracic neuromuscular scoliosis due to friedreich’s ataxia
Thoracic scoliosis due to friedreichs ataxia
Thoracolumbar neuromuscular scoliosis due to friedreich’s ataxia
Thoracolumbarscoliosis due to friedreichs ataxia
A condition marked by progressive cerebellar ataxia combined with myoclonus usually presenting in the third decade of life or later. Additional clinical features may include generalized and focal seizures, spasticity, and dyskinesias. Autosomal recessive and autosomal dominant patterns of inheritance have been reported. Pathologically, the dentate nucleus and brachium conjunctivum of the cerebellum are atrophic, with variable involvement of the spinal cord, cerebellar cortex, and basal ganglia. from Joynt, Clinical Neurology, 1991, ch37, pp60-1)
G11.1 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
The 2023 edition of ICD-10-CM G11.1 became effective on October 1, 2022.
This is the American ICD-10-CM version of G11.1 – other international versions of ICD-10 G11.1 may differ.