icd 10 code for x-thalassemia minor

by Jacques Buckridge 6 min read

ICD-10 code D56. 3 for Thalassemia minor is a medical classification as listed by WHO under the range - Diseases of the blood
Diseases of the blood
Hematologic diseases are disorders which primarily affect the blood & blood-forming organs. Hematologic diseases include rare genetic disorders, anemia, HIV, sickle cell disease & complications from chemotherapy or transfusions.
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and blood-forming organs and certain disorders involving the immune mechanism .

What is the ICD 10 code for thalassemia minor?

Thalassemia minor. D56.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2018/19 edition of ICD-10-CM D56.3 became effective on October 1, 2018. This is the American ICD-10-CM version of D56.3 - other international versions of ICD-10 D56.3 may differ.

What are the symptoms of thalassemia?

If you have thalassemia, your body has problems making hemoglobin, the protein in red blood cells that carries oxygen through your body. 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.

What are the treatment options for severe thalassemia?

Severe thalassemia is treated with blood transfusions and treatment to remove excess iron in the blood. ICD-10-CM D56.9 is grouped within Diagnostic Related Group (s) (MS-DRG v38.0): 791 Prematurity with major problems 793 Full term neonate with major problems

What is the ICD 10 code for anemia?

Diagnosis Index entries containing back-references to D56.9: Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9 ICD-10-CM Diagnosis Code D64.9 Arthritis, arthritic (acute) (chronic) (nonpyogenic) (subacute) M19.90 ICD-10-CM Diagnosis Code M19.90

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What is the ICD 10 code for thalassemia?

D56. 9 - Thalassemia, unspecified | ICD-10-CM.

Is thalassemia autosomal or X linked?

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.

What is a thalassemia minor?

In Thalassemia minor, the hemoglobin genes are inherited during conception, one from the mother (egg) and one from the father (sperm). People with a Thalassemia trait in one gene are known as carriers or are said to have thalassemia minor.

Is thalassemia minor the same as anemia?

Persons with thalassemia minor have (at most) mild anemia (slight lowering of the hemoglobin level in the blood). This situation can very closely resemble that with mild iron-deficiency anemia. However, persons with thalassemia minor have a normal blood iron level (unless they are iron deficient for other reasons).

What are the 4 types of thalassemia?

Alpha thalassemia occurs when some or all of the 4 genes that make hemoglobin (the alpha-globin genes) are missing or damaged....There are 4 types of alpha thalassemia:Alpha thalassemia silent carrier. ... Alpha thalassemia carrier. ... Hemoglobin H disease. ... Alpha thalassemia major.

Is thalassemia minor recessive or dominant?

Disease at a Glance Beta Thalassemia is caused by changes in the HBB gene while alpha Thalassemia is caused by genetic changes in the HBA1 and/or HBA2 genes. Both are inherited in an autosomal recessive manner.

Is thalassemia minor Alpha or beta?

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.

Is thalassemia a beta minor?

Thalassemia minima is mild and causes no problems. But you will be a carrier of the disorder. Thalassemia intermedia can cause problems based on the severity of the anemia. These problems include delayed growth, weak bones, and enlarged spleen.

How do you identify minor thalassemia?

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.

What is the difference between beta thalassemia major and minor?

Someone who inherits a beta thalassemia mutation from one parent has beta thalassemia trait (beta thalassemia minor). Someone who inherits a beta thalassemia mutation from each parent has beta thalassemia intermedia or beta thalassemia major (Cooley's anemia).

Is thalassemia trait the same as thalassemia minor?

People who have thalassemia trait (also called thalassemia minor) carry the genetic trait for thalassemia but do not usually experience any health problems except perhaps a mild anemia. A person may have either alpha thalassemia trait or beta thalassemia trait, depending upon which form of beta protein is lacking.

Is thalassemia minor a chronic disease?

It is known as alpha thalassemia minor. Three mutated genes: The person has hemoglobin H disease, a type of chronic anemia. They will need regular blood transfusions throughout their life.

What is postpartum thalassemia?

Thalassemia in pregnancy. Thalassemia postpartum. Clinical Information. A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains.

How does thalassemia affect the body?

If you have thalassemia, your body has problems making hemoglobin, the protein in red blood cells that carries oxygen through your body. 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. It mainly affects people of mediterranean or asian ancestry. It usually appears during the first two years of life. Severe thalassemia is treated with blood transfusions and treatment to remove excess iron in the blood.

When will the ICd 10 D56.9 be released?

The 2022 edition of ICD-10-CM D56.9 became effective on October 1, 2021.

When does thalassemia appear?

It usually appears during the first two years of life. Severe thalassemia is treated with blood transfusions and treatment to remove excess iron in the blood. Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

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.

Can D56 be used for reimbursement?

D56 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.

When will the ICd 10 D56.8 be released?

The 2022 edition of ICD-10-CM D56.8 became effective on October 1, 2021.

What is D50-D89?

D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

What is thalassemia alpha plus?

Thalassemia, alpha, homozygous. Clinical Information. 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.

When will the ICd 10 D56.0 be released?

The 2022 edition of ICD-10-CM D56.0 became effective on October 1, 2021.

What does a type 1 exclude note mean?

They must be used in conjunction with an underlying condition code and they must be listed following the underlying condition. 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 D56.0.

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