What is the ICD 10 code for Factor V Leiden?
What is the ICD 10 code for Factor V Leiden?
Factor v leiden mutation (r506q) is the most common cause of apc resistance. An abnormality that refers to mutation of factor v leiden, which is a variant of human factor v. It results in thrombophilia, deep vein thrombosis, and a slightly increased risk of miscarriage.
What is E72 12?
12 is a billable ICD code used to specify a diagnosis of methylenetetrahydrofolate reductase deficiency. A ‘billable code’ is detailed enough to be used to specify a medical diagnosis.
What is the ICD 10 code for hyperhomocysteinemia?
E72. 11 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
What is the difference between Factor V and Factor V Leiden?
What is Factor V Leiden Mutation? Factor V Leiden is a common change in a gene that controls a protein called Factor V. Factor V is a protein involved in blood clotting and the Factor V Leiden gene change (also called mutation) is linked to an increase risk of blood clots.
What is Factor V Leiden?
Factor V Leiden (FAK-tur five LIDE-n) is a mutation of one of the clotting factors in the blood. This mutation can increase your chance of developing abnormal blood clots, most commonly in your legs or lungs. Most people with factor V Leiden never develop abnormal clots.
What is the ICD-10-CM code for Mthfr mutation?
Names and Codes
| 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 |
What is heterozygous methylenetetrahydrofolate reductase mutation?
It might look like a curse word at first glance, but it actually 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.
What diagnosis will covers a homocysteine?
Homocysteine levels will be covered by Medicare to confirm vitamin B12 or folate deficiency.
What is homocysteine and what is its function?
Homocysteine is an amino acid. Vitamins B12, B6 and folate break down homocysteine to create other chemicals your body needs. High homocysteine levels may mean you have a vitamin deficiency. Without treatment, elevated homocysteine increases your risks for dementia, heart disease and stroke.
What type of mutation is Factor V Leiden?
Factor V Leiden is the name of a specific gene mutation that results in thrombophilia, which is an increased tendency to form abnormal blood clots that can block blood vessels.
What should you avoid with Factor V Leiden?
If your factor V Leiden requires you to take anticoagulant medication, here are some steps that might help you prevent injury and avoid excessive bleeding:
- Avoid playing contact sports or engaging in other activities that could result in physical injury.
- Use a soft toothbrush and waxed floss.
Is Factor V Leiden mutation an autoimmune disease?
Examples include abnormalities in Protein C, Protein S, Antithrombin, and Prothrombin 20210. Another disorder which leads to increased clotting is the Anti-Phospholipid Syndrome. This is an autoimmune disorder in which one’s own immune system attacks normal anti-clotting mechanisms.
What is methylenetetrahydrofolate reductase?
Methylenetetrahydrofolate Reductase (MTHFR), DNA Mutation Analysis – Reduced methylenetetrahydrofolate reductase (MTHFR) enzyme activity is a genetic risk factor for hyperhomocysteinemia, especially when present with low serum folate levels. Two common variants in the MTHFR gene result in reduced enzyme activity.
What is the ICD 10 code for methylenetetrahydrofolate deficiency?
Diagnosis Code E72.12. ICD-10: E72.12. Short Description: Methylenetetrahydrofolate reductase deficiency. Long Description: Methylenetetrahydrofolate reductase deficiency. This is the 2019 version of the ICD-10-CM diagnosis code E72.12. Valid for Submission. The code E72.12 is valid for submission for HIPAA-covered transactions.
What is the ICD-9 code for MTHFR?
The following ICD-9 codes for MTHFR are listed as a convenience for the ordering physician. The ordering physician should report the diagnosis code that best describes the reason for performing the test and provide the 4th and 5th ICD-9 digit as appropriate. MTHFR CPT Code 81291 Sample Type EDTA Whole Blood Order Code C605 Tube Type Lavender Top
What is the component test code for the MTHFR PCR?
Components Component Test Code* Component Chart Name LOINC 0055657 MTHFR Mutation: c.665C>T 28005-7 0055658 MTHFR Mutation: c.1286A>C 28060-2 0055660 MTHFR Interpretation 21709-1 2001331 MTHFR PCR Specimen 31208-2