icd 10 code for beta thalassemia trait

What is the ICD 10 code for delta beta thalassemia?

Oct 01, 2021 · D56.1 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 D56.1 became effective on October 1, 2021. This is the American ICD-10-CM version of D56.1 - other international versions of ICD-10 D56.1 may differ. Applicable To Beta thalassemia major Cooley's anemia

What is the ICD 10 code for Cooley's anemia?

Oct 01, 2021 · Thalassemia trait, beta Clinical Information A condition in which a person has reduced protein production from one of the four alpha-globin alleles. A condition in which a person has reduced protein production from two of the four alpha-globin alleles. ICD-10-CM D56.3 is grouped within Diagnostic Related Group (s) (MS-DRG v39.0):

What is the ICD 10 code for hemolytic anemia?

ICD-10-CM Code D56.1 Beta thalassemia BILLABLE | ICD-10 from 2011 - 2016 D56.1 is a billable ICD code used to specify a diagnosis of beta thalassemia. A 'billable code' is detailed enough to be used to specify a medical diagnosis. The ICD code D561 is used to code Beta thalassemia

What are the symptoms of thalassemia?

Oct 01, 2021 · D56.1 is a valid billable ICD-10 diagnosis code for Beta thalassemia. It is found in the 2022 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2021 - Sep 30, 2022 .

What is the ICD 10 code for thalassemia trait?

ICD-10-CM Code for Thalassemia minor D56. 3.

What is β-thalassemia trait?

Beta thalassemia is an inherited blood disorder in which the body doesn't make as much beta globin as it should. Beta globin and alpha globin are building blocks of hemoglobin. Hemoglobin is the part of red blood cell (RBC) that carries oxygen throughout the body.

Is beta thalassemia trait same as thalassemia minor?

Beta thalassemia trait is inherited from one's parents, like hair or eye color. Normally, beta thalassemia trait does not cause any health problems. Beta thalassemia trait is also known as beta thalassemia minor.

Is beta thalassemia carrier the same as trait?

If you're a carrier of thalassaemia, it means you carry one of the faulty genes that cause thalassaemia, but you do not have thalassaemia yourself. Being a carrier of the trait is sometimes known as having the thalassaemia trait or having thalassaemia minor.

How do you test for beta thalassemia trait?

Special blood tests called hemoglobin electrophoresis and quantitation of hemoglobin A2 and hemoglobin F are a reliable way of determining whether or not a person has the trait for beta thalassemia (beta thalassemia minor). These blood tests are available at most large hospitals and clinics.

How do you treat beta thalassemia trait?

Stem Cell Transplant "Hematopoietic" stem cells are young cells in your bone marrow -- the spongy center of your bones -- that grow into new blood cells. During a stem cell transplant, you get healthy blood-forming cells from a donor to replace your own damaged cells. A stem cell transplant can cure beta thalassemia.Nov 18, 2021

What happens if you have thalassemia trait?

Thalassemia (thal-uh-SEE-me-uh) is an inherited blood disorder that causes your body to have less hemoglobin than normal. Hemoglobin enables red blood cells to carry oxygen. Thalassemia can cause anemia, leaving you fatigued. If you have mild thalassemia, you might not need treatment.Nov 17, 2021

Can thalassemia trait turn into major?

Because the thalassemia trait is a genetic trait and not a health condition, it cannot "become worse" or change into one of the more serious forms of thalassemia that may require medical treatment.

Is thalassemia a dominant or recessive trait?

Inheritance. In general, thalassemia is inherited in an autosomal recessive manner; however, the inheritance can be quite complex as multiple genes can influence the production of hemoglobin. Most people affected by beta thalassemia have mutations in both copies of the HBB gene in each cell .

What is alpha thalassemia trait?

People with alpha thalassemia trait only have 2 genes for alpha globin, so their bodies make slightly less hemoglobin than normal. This trait was passed on from their parents, like hair color or eye color. A trait is different from a disease. Alpha thalassemia trait is not a disease.

What type of mutation is beta thalassemia?

Beta thalassemia major is caused by a homozygous mutation (beta-zero thalassemia) of the beta-globin gene, resulting in the total absence of beta chains. It manifests clinically as jaundice, growth retardation, hepatosplenomegaly, endocrine abnormalities, and severe anemia requiring life-long blood transfusions.Nov 5, 2021

What is beta plus thalassemia?

Sickle beta plus thalassemia (HbS β+thal) is a mild form of sickle cell disease. Many babies with HbS β+thal are born healthy and do not show symptoms until later in childhood. Some problems can include low red blood cell count, pain, and risk of infection.

What is thalassemia inherited?

An inherited form of anemia. Heterogeneous group of hereditary hemolytic anemias which have in common a decreased rate of synthesis of one or more hemoglobin polypeptide chains. If you have thalassemia, your body has problems making hemoglobin, the protein in red blood cells that carries oxygen through your body.

What does "type 1 excludes" mean?

A type 1 excludes note is a pure excludes. It means "not coded here". A type 1 excludes note indicates that the code excluded should never be used at the same time as D56. A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.

What is hemolytic anemia?

A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.

What is it called when you don't have enough oxygen?

When your blood does not carry enough oxygen to the rest of your body, you have anemia.thalassemia, a genetic disease, can be mild or severe. Some carriers of the gene have no symptoms. The most common severe form in the United States is a type called cooley's anemia.

Tabular List of Diseases and Injuries

The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code D56.1:

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 D56.1 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:

Clinical Information

BETA THALASSEMIA-. a disorder characterized by reduced synthesis of the beta chains of hemoglobin.

Information for Patients

Thalassemias are inherited blood disorders. If you have one, your body makes fewer healthy red blood cells and less hemoglobin. Hemoglobin is a protein that carries oxygen to the body. That leads to anemia. Thalassemias occur most often among people of Italian, Greek, Middle Eastern, Southern Asian, and African descent.