Valid for Submission
E88.40 is a billable diagnosis code used to specify a medical diagnosis of mitochondrial metabolism disorder, unspecified. The code E88.40 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 E88.40 might also be used to specify conditions or terms like demyelination of central nervous system co-occurrent and due to mitochondrial disease, hypertrophic mitochondrial cardiomyopathy, infantile hypertrophic cardiomyopathy due to mrpl44 deficiency, liver disease co-occurrent and due to mitochondrial disorder, mitochondrial cytopathy , mitochondrial metabolism defect, etc.
Unspecified diagnosis codes like E88.40 are acceptable when clinical information is unknown or not available about a particular condition. Although a more specific code is preferable, unspecified codes should be used when such codes most accurately reflect what is known about a patient's condition. Specific diagnosis codes should not be used if not supported by the patient's medical record.
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 E88.40 are found in the index:
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Demyelination of central nervous system co-occurrent and due to mitochondrial disease
- Hypertrophic mitochondrial cardiomyopathy
- Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
- Liver disease co-occurrent and due to mitochondrial disorder
- Mitochondrial cytopathy
- Mitochondrial metabolism defect
Convert E88.40 to ICD-9 Code
The General Equivalency Mapping (GEM) crosswalk indicates an approximate mapping between the ICD-10 code E88.40 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
Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive system (enzymes) break the food parts down into sugars and acids, your body's fuel. Your body can use this fuel right away, or it can store the energy in your body tissues. If you have a metabolic disorder, something goes wrong with this process.
Mitochondrial diseases are a group of metabolic disorders. Mitochondria are small structures that produce energy in almost all of your cells. They make it by combining oxygen with the fuel molecules (sugars and fats) that come from your food. When the mitochondria are defective, the cells do not have enough energy. The unused oxygen and fuel molecules build up in the cells and cause damage.
The symptoms of mitochondrial disease can vary. It depends on how many mitochondria are defective, and where they are in the body. Sometimes only one organ, tissue, or cell type is affected. But often the problem affects many of them. Muscle and nerve cells have especially high energy needs, so muscular and neurological problems are common. The diseases range from mild to severe. Some types can be fatal.
Genetic mutations cause these diseases. They usually happen before age 20, and some are more common in infants. There are no cures for these diseases, but treatments may help with symptoms and slow down the disease. They may include physical therapy, vitamins and supplements, special diets, and medicines.
[Learn More in MedlinePlus]