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ALL MEDICAL CODES IN CATEGORY Systemic atrophies primarily affecting the central nervous system

2025 ICD-10-CM code G12.25

Progressive spinal muscle atrophy (SMA) is an inherited neurological disorder causing progressive muscle weakness and wasting.

2025 ICD-10-CM code G12.21

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is a progressive neurodegenerative disease affecting motor neurons, causing muscle weakness, atrophy, and eventual loss of function.

2025 ICD-10-CM code G11.2

Late-onset cerebellar ataxia (LOCA).

2025 ICD-10-CM code G11.11

Friedreich ataxia

2025 ICD-10-CM code G11.4

Hereditary spastic paraplegia.

2025 ICD-10-CM code G12.0

Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]. This is the most severe form of spinal muscular atrophy (SMA), characterized by the degeneration and loss of motor neurons in the spinal cord and brainstem.

2025 ICD-10-CM code G11.10

Early-onset cerebellar ataxia, unspecified.

2025 ICD-10-CM code G11

Hereditary ataxia

2025 ICD-10-CM code G11.9

Hereditary ataxia, unspecified. This encompasses various genetic disorders causing impaired coordination and movement control, where the specific type is not documented.

2025 ICD-10-CM code G12

Spinal muscular atrophy and related syndromes

2025 ICD-10-CM code G11.3

Cerebellar ataxia with defective DNA repair (Ataxia telangiectasia [Louis-Bar]).

2025 ICD-10-CM code G11.1

Early-onset cerebellar ataxia (EOCA) is a genetic disorder characterized by progressive deterioration of gait, coordination, and voluntary movements beginning in childhood.

2025 ICD-10-CM code G10

Huntington's disease (HD) is a progressive neurodegenerative disorder characterized by uncontrolled movements, cognitive decline, and psychiatric symptoms.

2025 ICD-10-CM code G14

Postpolio syndrome.Includes: postpolio myelitic syndrome.

2025 ICD-10-CM code G13.1

Other systemic atrophy primarily affecting the central nervous system in neoplastic disease; this code is used when a neurological disorder in a cancer patient is not specified by another code.

2025 ICD-10-CM code G12.8

Other spinal muscular atrophies and related syndromes encompass a group of genetic disorders affecting motor neurons in the spinal cord, leading to muscle weakness.

2025 ICD-10-CM code G13.0

Paraneoplastic neuromyopathy and neuropathy; a neurological disorder secondary to cancer.

2025 ICD-10-CM code G12.20

Unspecified motor neuron disease; a group of neurological disorders affecting motor neurons, leading to muscle weakness.

2025 ICD-10-CM code G12.2

Motor neuron disease is a group of progressive neurological disorders causing muscle weakness and atrophy due to the degeneration of motor neurons.

2025 ICD-10-CM code G13.2

Systemic atrophy primarily affecting the central nervous system in myxedema.This code is for the manifestation of an underlying disease, not the disease itself.

2025 ICD-10-CM code G11.8

Other hereditary ataxias are a group of genetic disorders marked by uncontrolled voluntary movements, leading to staggering gait, poor coordination, and atypical movements.

2025 ICD-10-CM code G12.1

Other inherited spinal muscular atrophy (SMA); encompasses various SMA types not specified elsewhere.

2025 ICD-10-CM code G12.23

Primary lateral sclerosis (PLS) is a neurological disorder affecting upper motor neurons, causing progressive weakness and stiffness.

2025 ICD-10-CM code G12.24

Familial motor neuron disease is a rare inherited neurological disorder causing progressive muscle weakness.

2025 ICD-10-CM code G13

Systemic atrophies primarily affecting the central nervous system due to diseases classified elsewhere.

2025 ICD-10-CM code G12.22

Progressive bulbar palsy is a motor neuron disease affecting the brainstem, causing progressive weakness in muscles responsible for swallowing, speaking, and chewing.