icd 9 cm code for spinal muscular atrophy type 2

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What is the ICD 10 code for spinal muscular atrophy?

Spinal muscular atrophy, unspecified 1 G12.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 The 2021 edition of ICD-10-CM G12.9 became effective on October 1, 2020. 3 This is the American ICD-10-CM version of G12.9 - other international versions of ICD-10 G12.9 may differ. More ...

What is Spinal muscular atrophy (SMA)?

Spinal muscular atrophy (sma) is a genetic disease that attacks nerve cells, called motor neurons, in your spinal cord. These neurons communicate with your voluntary muscles - the ones you can control, like in your arms and legs.

What are the other inherited forms of spinal muscular atrophy?

Other inherited spinal muscular atrophy 1 Adult form spinal muscular atrophy 2 Childhood form, type II spinal muscular atrophy 3 Distal spinal muscular atrophy 4 Juvenile form, type III spinal muscular atrophy [Kugelberg-Welander] 5 Progressive bulbar palsy of childhood [Fazio-Londe] 6 Scapuloperoneal form spinal muscular atrophy

What are the symptoms of spinal muscular atrophy?

Spinal muscular atrophy, unspecified. Symptoms may appear at any age and include progressive loss of coordination of gait, hands, speech, and eye movements. Spinal muscular atrophy (sma) is a genetic disease that attacks nerve cells, called motor neurons, in your spinal cord. These neurons communicate with your voluntary muscles -...

What is the ICD-10-CM code for spinal muscular atrophy?

G12. 9 - Spinal muscular atrophy, unspecified | ICD-10-CM.

What is G12 9?

G12.9 - Spinal muscular atrophy, unspecified.

Which of the following codes are assigned for an adult patient with progressive spinal muscle atrophy inherited and anxiety?

Spinal muscular atrophy, unspecified G12. 9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM G12. 9 became effective on October 1, 2021.

Can F07 81 be used as a primary diagnosis?

Our physicians have used IDC-10 code F07. 81 as the primary diagnosis for patients presenting with post concussion syndrome.

What type of disease is spinal muscular atrophy?

Description. Spinal muscular atrophy is a genetic disorder characterized by weakness and wasting (atrophy ) in muscles used for movement (skeletal muscles). It is caused by a loss of specialized nerve cells, called motor neurons that control muscle movement.

Can B96 81 be used as a primary diagnosis?

The note in ICD-10 under codes B95-B97 states that 'these categories are provided for use as supplementary or additional codes to identify the infectious agent(s) in disease classified elsewhere', so you would not use B96. 81 as a primary diagnosis, but as an additional code with the disease listed first.

What is the term for a group of disorders marked by progressive degeneration of motor neurons in the spinal cord?

Diseases of the nervous system. Approximate Synonyms. Spinal muscular atrophy. Clinical Information. A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts.

What is the name of the disease that attacks the spinal cord?

Symptoms may appear at any age and include progressive loss of coordination of gait, hands, speech, and eye movements. Spinal muscular atrophy (sma) is a genetic disease that attacks nerve cells, called motor neurons, in your spinal cord.

What is the disease that attacks the nerve cells in the spinal cord?

Spinal muscular atrophy (sma) is a genetic disease that attacks nerve cells, called motor neurons, in your spinal cord. These neurons communicate with your voluntary muscles - the ones you can control, like in your arms and legs. As you lose the neurons, your muscles weaken. This can affect walking, crawling, breathing, ...

Can sma affect your family?

This can affect walking, crawling, breathing, swallowing and head and neck control.sma runs in families. Parents usually have no symptoms, but still carry the gene. Genetic counseling is important if the disease runs in your family.there are many types of sma, and some of them are fatal.