| Condition:1 | Methylene tetrahydrofolate reductase deficiency |
|---|---|
| SNOMED CT Code:3 | 41797007—5,10-Methylenetetrahydrofolate reductase deficiency UMLS CUI:4C0268615 |
| ICD-9-CM Code:5 | 270.4—Disturbances of sulphur-bearing amino-acid metabolism |
| ICD-10-CM Code:6 | E72.12—Methylenetetrahydrofolate reductase deficiency |
Oct 01, 2021 · Methylenetetrahydrofolate reductase deficiency. E72.12 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 E72.12 became effective on October 1, 2021.
ICD-10 code E72.12 for Methylenetetrahydrofolate reductase deficiency is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases . Subscribe to Codify and get the code details in a flash.
ICD-10-CM Code E72.12Methylenetetrahydrofolate reductase deficiency. ICD-10-CM Code. E72.12. Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis. E72.12 is a billable ICD code used to specify a diagnosis of methylenetetrahydrofolate reductase deficiency.
E72.12 is a billable diagnosis code used to specify a medical diagnosis of methylenetetrahydrofolate reductase deficiency. The code E72.12 is valid during the fiscal year 2022 from October 01, 2021 through September 30, 2022 for the submission of HIPAA-covered transactions. The ICD-10-CM code E72.12 might also be used to specify conditions or terms …
Methylenetetrahydrofolate Reductase (MTHFR) Deficiency is the most common genetic cause of elevated levels of homocysteine in the plasma (hyperhomocysteinemia). The MTHFR enzyme plays an important role in processing amino acids, specifically, the conversion of homocysteine to methionine.Mar 8, 2012
It refers to a relatively common genetic mutation. MTHFR stands for methylenetetrahydrofolate reductase. It's getting attention due to a genetic mutation that may lead to high levels of homocysteine in the blood and low levels of folate and other vitamins.
Valid for SubmissionICD-10:E72.12Short Description:Methylenetetrahydrofolate reductase deficiencyLong Description:Methylenetetrahydrofolate reductase deficiency
E72.11ICD-10 | Homocystinuria (E72. 11)
5-MTHF plays an essential role in methylation, it enables the conversion of homocysteine to methionine, the production of serotonin and melatonin, and it is indirectly involved in the synthesis of DNA.
The MTHFR mutation will also cause issues with detoxing properly, as well as issues with hormone balance and immune system function. It has been associated with autoimmune conditions such as fibromyalgia, Hashimoto's, and lupus.Aug 31, 2020
E72. 11 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Risk factors People inherit one copy of the MTHFR gene from each of their parents, which means that everyone has two MTHFR genes. Mutations can occur in one or both of these genes. Having a parent or close relative with an MTHFR gene mutation can increase a person's risk of inheriting the same variant themselves.Jan 3, 2020
511238: Methylenetetrahydrofolate Reductase (MTHFR) Thermolabile Variant, DNA Analysis | Labcorp.
83 – Other Fatigue. Code R53. 83 is the diagnosis code used for Other Fatigue.
Homocysteine is an amino acid produced when proteins are broken down. A high homocysteine level, also called hyperhomocysteinemia, can contribute to arterial damage and blood clots in your blood vessels. High homocysteine levels usually indicate a deficiency in vitamin B-12 or folate.
Code D64. 9 is the diagnosis code used for Anemia, Unspecified, it falls under the category of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
Cystathioninuria, also called cystathionase deficiency, is an autosomal recessive metabolic disorder that results in an excess of cystathionine in the urine. It is associated with a congenital dysfunction of the enzyme cystathionase, or acquired deficiency of vitamin B6 which is essential for the function of this enzyme.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E72.12. Click on any term below to browse the alphabetical index.
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code E72.12 and a single ICD9 code, 270.4 is an approximate match for comparison and conversion purposes.
The General Equivalency Mapping (GEM) crosswalk indicates an approximate mapping between the ICD-10 code E72.12 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. Amino Acid Metabolism Disorders. Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Your digestive system breaks the food parts down into sugars and acids, your body's fuel.
If you have a metabolic disorder, something goes wrong with this process. One group of these disorders is amino acid metabolism disorders. They include phenylketonuria (PKU) and maple syrup urine disease. Amino acids are "building blocks" that join together to form proteins.
Amino acids are "building blocks" that join together to form proteins. If you have one of these disorders, your body may have trouble breaking down certain amino acids. Or there may be a problem getting the amino acids into your cells. These problems cause a buildup of harmful substances in your body.
The most common form of homocystinuria is characterized by nearsightedness (myopia), dislocation of the lens at the front of the eye, an increased risk of abnormal blood clotting, and brittle bones that are prone to fracture (osteoporosis) or other skeletal abnormalities.