icd 10 code for mitochondrial defect

What is the ICD 10 code for mitochondrial metabolism disorder?

Mitochondrial metabolism disorder, unspecified. E88.40 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM E88.40 became effective on October 1, 2018.

What is the ICD 10 code for chondromalacia?

E88.40 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2020 edition of ICD-10-CM E88.40 became effective on October 1, 2019.

What is the ICD 10 code for excluded note?

G71.3 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 G71.3 became effective on October 1, 2021. This is the American ICD-10-CM version of G71.3 - other international versions of ICD-10 G71.3 may differ. A type 1 excludes note is a pure excludes.

What is the ICD 9 code for MELAS syndrome?

Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS syndrome) 277.87 MELAS (mitochondrial encephalopathy, lactic acidosis and stroke-like episodes) 277.87 ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions.

What is mitochondrial metabolism defect?

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.

What is the ICD-10 code for mitochondrial myopathy?

ICD-10 code: G71. 3 Mitochondrial myopathy, not elsewhere classified.

What are the symptoms of mitochondrial myopathy?

The symptoms of mitochondrial myopathies include muscle weakness or exercise intolerance, heart failure or rhythm disturbances, dementia, movement disorders, stroke-like episodes, deafness, blindness, droopy eyelids, limited mobility of the eyes, vomiting, and seizures.

How is mitochondrial dysfunction diagnosed?

How are mitochondrial diseases diagnosed?A review of a patient's family history.A complete physical examination.A neurological examination.A metabolic examination that includes blood and urine tests, and, if needed, a cerebral spinal fluid test (spinal tap).

How does mitochondrial disease affect the body?

Mitochondrial disease can cause a vast array of health concerns, including fatigue, weakness, metabolic strokes, seizures, cardiomyopathy, arrhythmias, developmental or cognitive disabilities, diabetes mellitus, impairment of hearing, vision, growth, liver, gastrointestinal, or kidney function, and more.

What is mitochondrial Cytopathy?

Mitochondrial cytopathies represent a heterogeneous group of multisystem disorders which preferentially affect the muscle and nervous systems. They are caused either by mutations in the maternally inherited mitochondrial genome, or by nuclear DNA-mutations.

How many types of mitochondrial disorders are there?

There are nine main forms of mitochondrial myopathy: Kearns-Sayre syndrome (KSS) Leigh syndrome. Mitochondrial DNA (mtDNA) depletion syndrome.

Which of the following is a mitochondrial disorder?

Common clinical features of mitochondrial disorders include ptosis, external ophthalmoplegia, proximal myopathy and exercise intolerance, cardiomyopathy, sensorineural deafness, optic atrophy, pigmentary retinopathy, and diabetes mellitus.

What are primary mitochondrial disorders?

Primary mitochondrial myopathies (PMM) are a group of disorders that are associated with changes in genetic material (e.g. depletions, deletions, or mutations) found within the DNA of mitochondria (mtDNA) or with genes outside the mitochondria (nuclear DNA), affecting predominantly the skeletal muscle.

What causes mitochondrial dysfunction?

What causes mitochondrial dysfunction? On a physiological level, mitochondrial dysfunction is caused by exposure to certain environmental factors (such as certain pharmaceutical drugs, occupational chemicals and cigarette smoke) or genetic abnormalities (of both mitochondrial and nuclear DNA).

What causes mitochondrial disease?

Mitochondrial diseases are not contagious, and they are not caused by anything a person does. They're caused by mutations, or changes, in genes — the cells' blueprints for making proteins.

How is mitochondrial disease diagnosed in adults?

For a specific clinical syndrome, a non-invasive genetic test might be possible on blood, urine or buccal mucosa. However, if these tests return negative, or the clinical features in the first instance necessitate a muscle biopsy (eg CPEO), then this is most commonly undertaken.

How long can you live with mitochondrial myopathy?

Typically, the age of death is between 10 to 35 years, although some patients may live longer. Death may come as a result of general body wasting due to progressive dementia and muscle weakness, or complications from other affected organs such as heart or kidneys.

What are the signs and symptoms of myopathy?

What are the symptoms of myopathy?Muscle weakness, most commonly of your upper arms and shoulders and thighs (more common and more severe).Muscle cramps, stiffness and spasms.Fatigue with exertion.Lack of energy.

Is mitochondrial myopathy painful?

Chronic pain is common in patients with mitochondrial disease. Pain due to mitochondrial disease is primarily of neuropathic nature. Distribution, intensity and type of pain are genetically determined.

What is the most common mitochondrial disease?

Together, Leigh syndrome and MELAS are the most common mitochondrial myopathies. The prognosis of Leigh syndrome is generally poor, with survival generally being a matter of months after disease onset.

Coding Notes for E88.4 Info for medical coders on how to properly use this ICD-10 code

Type-1 Excludes mean the conditions excluded are mutually exclusive and should never be coded together. Excludes 1 means "do not code here."

ICD-10-CM Alphabetical Index References for 'E88.4 - Mitochondrial metabolism disorders'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E88.4. Click on any term below to browse the alphabetical index.