Valid for Submission
G12.8 is a billable diagnosis code used to specify a medical diagnosis of other spinal muscular atrophies and related syndromes. The code G12.8 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions.
The ICD-10-CM code G12.8 might also be used to specify conditions or terms like bulbospinal neuronopathy, facioscapulohumeral spinal muscular atrophy, facioscapulohumeral spinal muscular atrophy with sensory loss or oculopharyngeal spinal muscular atrophy.
Index to Diseases and Injuries
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code G12.8 are found in the index:
- - Atrophy, atrophic (of)
- - Cruveilhier's atrophy or disease - G12.8
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Bulbospinal neuronopathy
- Facioscapulohumeral spinal muscular atrophy
- Facioscapulohumeral spinal muscular atrophy with sensory loss
- Oculopharyngeal spinal muscular atrophy
Convert G12.8 to ICD-9 Code
The General Equivalency Mapping (GEM) crosswalk indicates an approximate mapping between the ICD-10 code G12.8 its ICD-9 equivalent. The approximate mapping means there is not an exact match between the ICD-10 code and the ICD-9 code and the mapped code is not a precise representation of the original code.
Information for Patients
Spinal Muscular Atrophy
Also called: SMA
Spinal muscular atrophy (SMA) is a genetic disease that attacks nerve cells, called motor neurons, in the spinal cord. These cells communicate with your voluntary muscles - the ones you can control, like in your arms and legs. As the neurons die, the muscles weaken. 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. Some of them are fatal. Some people have a normal life expectancy. It depends on the type and how it affects breathing. There is no cure. Treatments help with symptoms and prevent complications. They may include machines to help with breathing, nutritional support, physical therapy, and medicines.
NIH: National Institute of Neurological Disorders and Stroke
- Spinal muscular atrophy (Medical Encyclopedia)
- Swallowing problems (Medical Encyclopedia)
[Learn More in MedlinePlus]