icd 10 code for prothrombin gene mutation

What gene or chromosome is mutated in this disorder?

Oct 01, 2021 · Prothrombin gene mutation. 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code. D68.52 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 D68.52 became effective on October 1, 2021.

Is MTHFR gene mutation clinically significant?

ICD-10-CM Code for Prothrombin gene mutation D68.52 ICD-10 code D68.52 for Prothrombin gene mutation is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .

What type of gene mutation causes sickle cell anemia?

Oct 01, 2021 · Prothrombin gene mutation Billable Code. D68.52 is a valid billable ICD-10 diagnosis code for Prothrombin gene mutation . It is found in the 2021 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2020 - …

What type of gene is mutated in cystic fibrosis?

10 result found: ICD-10-CM Diagnosis Code D68.52 [convert to ICD-9-CM] Prothrombin gene mutation. Prothrombin g20210a mutation. ICD-10-CM Diagnosis Code D68.52. Prothrombin gene mutation. 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code.

What is prothrombin gene mutation?

What is prothrombin gene mutation? Prothrombin gene mutation (or Factor II mutation or Prothrombin G20210A) is an inherited condition that increases your predisposition to develop abnormal blood clots in the veins (deep vein thrombosis or DVT) and lungs (pulmonary embolism or PE).Sep 28, 2021

What is prothrombin gene mutation heterozygous?

Heterozygous: You have inherited one copy of the prothrombin gene mutation, from one parent. The other copy of the prothrombin gene, inherited from your other parent, is normal.

What is the ICD 10 for Factor V Leiden mutation?

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.

Is prothrombin gene mutation a bleeding disorder?

Prothrombin 20210 Mutation, also called Factor II Mutation is a genetic condition that causes an increase in the likelihood of your blood forming dangerous blood clots. All individuals make the prothrombin (also called factor two) protein that helps blood clot.

Is Factor V the same as prothrombin gene mutation?

Symptoms of Factor V Leiden and Prothrombin Gene Mutation Both factor V Leiden and a prothrombin gene mutation do not have symptoms on their own, and some people may never know that they have them. But it is important for anyone to know the symptoms of blood clots, DVT, and pulmonary embolism.Nov 18, 2020

What do you do if you have a prothrombin mutation?

Is there any treatment for Prothrombin Gene Mutation? No treatment to change genes is currently available. Most people who have the Prothrombin Gene Mutation do not require any treatment but need to be careful at times when the risk of getting a blood clot may be increased (e.g. after surgery, during long flights etc).

What diagnosis code will cover Factor V Leiden?

Group 1CodeDescription81241F5 (COAGULATION FACTOR V) (EG, HEREDITARY HYPERCOAGULABILITY) GENE ANALYSIS, LEIDEN VARIANT81291MTHFR (5,10-METHYLENETETRAHYDROFOLATE REDUCTASE) (EG, HEREDITARY HYPERCOAGULABILITY) GENE ANALYSIS, COMMON VARIANTS (EG, 677T, 1298C)1 more row

What is prothrombin factor?

Prothrombin is a protein in the blood that is required for the blood to clot. It is also called factor II. Blood clots are composed of a combination of blood platelets and a meshwork of the blood clotting protein fibrin. Prothrombin is a blood clotting protein that is needed to form fibrin.

What does Hypercoagulability mean?

Introduction. Hypercoagulability or thrombophilia is the increased tendency of blood to thrombose. A normal and healthy response to bleeding for maintaining hemostasis involves the formation of a stable clot, and the process is called coagulation.Sep 29, 2021

Is Prothrombin gene mutation dominant?

Prothrombin-related thrombophilia is inherited in an autosomal dominant pattern. All individuals inherit two copies of each gene .

Can I donate blood with Prothrombin gene mutation?

People with factor V Leiden may donate blood, platelets or plasma safely, as long as they are not on an anticoagulant such as warfarin. Only a very few medicines prevent people from donating blood.

Can you have a baby with Prothrombin gene mutation?

The second most common genetic type is prothrombin thrombophilia, which mainly affects people of European ancestry. It involves a mutation in the F2 gene. Genetic types of thrombophilia may raise the risk of multiple miscarriages, but most women with these genetic mutations have normal pregnancies.

What is the ICd 10 code for Prothrombin?

D68.52 is a valid billable ICD-10 diagnosis code for Prothrombin gene mutation . It is found in the 2021 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2020 - Sep 30, 2021 .

What does "excludes2" mean?

An Excludes2 note indicates that the condition excluded is not part of the condition it is excluded from but a patient may have both conditions at the same time. When an Excludes2 note appears under a code it is acceptable to use both the code and the excluded code together.

What is tabular list?

When a specific code is not available for a condition, the Tabular List includes an NEC entry under a code to identify the code as the “other specified” code. This abbreviation is the equivalent of unspecified. This note further define, or give examples of, the content of the code or category.

What is a list of terms?

List of terms is included under some codes. These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of “other specified” codes, the terms are a list of the various conditions assigned to that code.

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 D68.52 are found in the index:

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

Convert D68.52 to ICD-9 Code

The General Equivalency Mapping (GEM) crosswalk indicates an approximate mapping between the ICD-10 code D68.52 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

Normally, if you get hurt, your body forms a blood clot to stop the bleeding. For blood to clot, your body needs cells called platelets and proteins known as clotting factors. If you have a bleeding disorder, you either do not have enough platelets or clotting factors or they don't work the way they should.