icd 10 code for possible thalassemia

by Prof. Rex Rempel 5 min read

Thalassemia, unspecified
D56. 9 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. 9 became effective on October 1, 2021.

What is the ICD 10 code for alpha thalassemia?

Alpha thalassemia. D56.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM D56.0 became effective on October 1, 2018.

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 Cooley's anemia?

Diagnosis Index entries containing back-references to D56.1: Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9 ICD-10-CM Diagnosis Code D64.9 Cooley's anemia D56.1 Thalassemia (anemia) (disease) D56.9 ICD-10-CM Diagnosis Code D56.9

image

What is the ICD 10 code for thalassemia minor?

ICD-10 code D56. 3 for Thalassemia minor 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 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.

What are the three types of thalassemia?

When you have beta thalassemia, your body doesn't make enough protein in red blood cells called hemoglobin. That makes it hard for oxygen to get to all of your body's cells. There are three main types of the disease: beta thalassemia major, intermedia, and minor.

What is thalassemia major and minor?

Beta-thalassemia One mutated gene, you'll have mild signs and symptoms. This condition is called thalassemia minor or beta-thalassemia. Two mutated genes, your signs and symptoms will be moderate to severe. This condition is called thalassemia major, or Cooley anemia.

What is the difference between anemia and thalassemia?

Anemia is a condition in which your body doesn't have enough normal, healthy red blood cells. Thalassemia is inherited, meaning that at least one of your parents must be a carrier of the disorder. It's caused by either a genetic mutation or a deletion of certain key gene fragments.

What is the difference between alpha thalassemia and beta thalassemia?

The thalassemias are a group of inherited hematologic disorders caused by defects in the synthesis of one or more of the hemoglobin chains. Alpha thalassemia is caused by reduced or absent synthesis of alpha globin chains, and beta thalassemia is caused by reduced or absent synthesis of beta globin chains.

What are the two major types of thalassemia?

There are two main types of thalassemia:Alpha thalassemia occurs when a gene or genes related to the alpha globin protein are missing or changed (mutated).Beta thalassemia occurs when similar gene defects affect production of the beta globin protein.

Which thalassemia is most common?

Frequency. Beta thalassemia is a fairly common blood disorder worldwide. Thousands of infants with beta thalassemia are born each year. Beta thalassemia occurs most frequently in people from Mediterranean countries, North Africa, the Middle East, India, Central Asia, and Southeast Asia.

How is thalassemia diagnosis?

Doctors diagnose thalassemias using blood tests, including a complete blood count (CBC) and special hemoglobin tests.A CBC measures the amount of hemoglobin and the different kinds of blood cells, such as red blood cells, in a sample of blood. ... Hemoglobin tests measure the types of hemoglobin in a blood sample.

How is thalassemia minor 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.

Is beta thalassemia the same as thalassemia minor?

Why is it important to know if I have beta thalassemia trait? 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.

What is beta thalassemia minor?

What is beta thalassemia? Thalassemia (thal-uh-SEE-mee-uh) is a blood disorder that is inherited. This means it is passed down from one or both parents through their genes. When you have thalassemia, your body makes less hemoglobin than normal. Hemoglobin is an iron-rich protein in red blood cells.