icd 10 code for alpha thalassemia

What is the ICD-10-CM code for thalassemia?

Oct 01, 2021 · Alpha thalassemia. D56.0 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 D56.0 became effective on October 1, 2021. This is the American ICD-10-CM version of D56.0 - other international versions of ICD-10 D56.0 may differ.

What is the ICD 10 code for hydrops fetalis due to alpha thalassemia?

Alpha thalassemia (D56.0) D56 D56.0 D56.1 ICD-10-CM Code for Alpha thalassemia D56.0 ICD-10 code D56.0 for Alpha thalassemia 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 . Subscribe to Codify and get the code details in a flash.

What is the pathophysiology of alpha thalassemia?

Oct 01, 2021 · D56.0. D56.0 is a valid billable ICD-10 diagnosis code for Alpha 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 diagnosis D56?

Alpha thalassemia BILLABLE | ICD-10 from 2011 - 2016 D56.0 is a billable ICD code used to specify a diagnosis of alpha thalassemia. A 'billable code' is detailed enough to be used to specify a medical diagnosis. The ICD code D560 is used to code Alpha-thalassemia

What is alpha thalassemia?

Alpha thalassemia is a blood disorder that reduces the production of hemoglobin . Hemoglobin is the protein in red blood cells that carries oxygen to cells throughout the body.

What are the 4 types of alpha thalassemia?

There are 4 types of alpha thalassemia:Alpha thalassemia silent carrier. One gene is missing or damaged, and the other 3 are normal. Blood tests are usually normal. ... Alpha thalassemia carrier. Two genes are missing. ... Hemoglobin H disease. Three genes are missing. ... Alpha thalassemia major. All 4 genes are missing.

What is alpha thalassemia minor?

Alpha thalassemia carrier. A person who is a carrier has no signs or symptoms of anemia. They don't need any special medical treatment. Alpha thalassemia trait (also called alpha thalassemia minor). People with alpha thalassemia minor may have mild anemia, but usually don't need any medical treatment.

Is alpha thalassemia a sickle cell disease?

Alpha-thalassemia is related to prolonged survival in sickle cell anemia. Blood 1983; 62:286.Aug 8, 2021

How do alpha and beta thalassemia differ?

If either the alpha or beta part is not made, there aren't enough building blocks to make normal amounts of hemoglobin. Low alpha is called alpha thalassemia. Low beta is called beta thalassemia. When the words “trait,” “minor,” “intermedia,” or “major” are used, these words describe how severe the thalassemia is.

How do you diagnose alpha thalassemia?

The following blood tests are done to check for the condition and to tell if you are a carrier and can pass the disorder on to your children:Complete blood count (CBC). This test checks the size, number, and maturity of different blood cells in a set volume of blood.Hemoglobin electrophoresis. ... Ferritin. ... DNA testing.

What is alpha gene?

The HBA1 gene provides instructions for making a protein called alpha-globin. This protein is also produced from a nearly identical gene called HBA2. These two alpha-globin genes are located close together in a region of chromosome 16 known as the alpha-globin locus.Sep 28, 2020

What does microcytosis 1+ mean?

Microcytosis is typically an incidental finding in asymptomatic patients who received a complete blood count for other reasons. The condition is defined as a mean corpuscular volume of less than 80 μm3 (80 fL) in adults. The most common causes of microcytosis are iron deficiency anemia and thalassemia trait.Nov 1, 2010

How is thalassemia diagnosis?

If your doctor suspects your child has thalassemia, he or she can confirm a diagnosis with blood tests. Blood tests can reveal the number of red blood cells and abnormalities in size, shape or color. Blood tests can also be used for DNA analysis to look for mutated genes.Nov 17, 2021

What is b 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.

What is thalassemia?

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.Nov 17, 2021

Is thalassemia dominant or recessive?

Inheritance. Thalassemia major and thalassemia intermedia are inherited in an autosomal recessive pattern , which means both copies of the HBB gene in each cell have mutations.

The ICD code D560 is used to code Alpha-thalassemia

Alpha-thalassemia (α-thalassemia, α-thalassaemia) is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of alpha chains from 1,2,3, or all 4 of the alpha globin genes, leading to a relative excess of beta globin chains.

Coding Notes for D56.0 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.

ICD-10-CM Alphabetical Index References for 'D56.0 - Alpha thalassemia'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D56.0. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 282.43 was previously used, D56.0 is the appropriate modern ICD10 code.

What is Alpha Thalassemia?

ALPHA THALASSEMIA-. a disorder characterized by reduced synthesis of the alpha chains of hemoglobin. the severity of this condition can vary from mild anemia to death depending on the number of genes deleted.

What is the most common type of anemia?

Some people have no symptoms or mild anemia. The most common severe type in the United States is called Cooley's anemia. It usually appears during the first two years of life. People with it may have severe anemia, slowed growth and delayed puberty, and problems with the spleen, liver, heart, or bones.

What does "use additional code" mean?

The “use additional code” indicates that a secondary code could be used to further specify the patient’s condition. This note is not mandatory and is only used if enough information is available to assign an additional code.

What is a type 1 exclude note?

Type 1 Excludes. A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!". An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note.

What is the blood disorder that reduces the production of hemoglobin?

Alpha thalassemia Alpha thalassemia is a blood disorder that reduces the production of hemoglobin. Hemoglobin is the protein in red blood cells that carries oxygen to cells throughout the body.In people with the characteristic features of alpha thalassemia, a reduction in the amount of hemoglobin prevents enough oxygen from reaching ...

What is the treatment for iron deficiency?

Treatments include blood transfusions and treatment to remove excess iron from the body. If you have mild symptoms or no symptoms, you may not need treatment. In some severe cases, you may need a bone marrow transplant. Alpha thalassemia Alpha thalassemia is a blood disorder that reduces the production of hemoglobin.