icd 9 code for beta thalessemia

What is the ICD 10 code for beta thalassemia?

ICD-10 code D56. 1 for Beta 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 .

What is β Thalassaemia?

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.

What is the ICD 9 code for thalassemia?

ICD-9 Code 282.4 -Thalassemias- Codify by AAPC.

What is the ICD 10 code for thalassemia?

D56. 9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

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 the difference between alpha thalassemia and beta thalassemia?

When thalassemia is called “alpha” or “beta,” this refers to the part of hemoglobin that isn't being made. 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.

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 ICD-10 code for anemia?

Code D64. 9 is the diagnosis code used for Anemia, Unspecified, it falls under the category of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism. Anemia specifically, is a condition in which the number of red blood cells is below normal.

What is alpha 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. One gene is missing or damaged, and the other 3 are normal. Blood tests are usually normal.

What is Hb E beta thalassemia?

Hb E/β-thalassemia, which is the most serious form of Hb E syndromes, is a condition that results from the coinheritance of a β-thalassemia minor trait from one parent and Hb E from the other. It ranges from mild to severe thalassemia of the transfusion-dependent type.

What is the ICD 10 code for elevated hemoglobin?

ICD-10-CM Diagnosis Code R97 R97.

What is the ICD 10 code for Microcytosis?

Other abnormality of red blood cells The 2022 edition of ICD-10-CM R71. 8 became effective on October 1, 2021. This is the American ICD-10-CM version of R71.

Not Valid for Submission

282.49 is a legacy non-billable code used to specify a medical diagnosis of other thalassemia. This code was replaced on September 30, 2015 by its ICD-10 equivalent.

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.

ICD-9 Footnotes

General Equivalence Map Definitions The ICD-9 and ICD-10 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

What is the ICd code for thalassemia?

The ICD code D561 is used to code Beta thalassemia. Beta thalassemias (β thalassemias) are a group of inherited blood disorders. They are caused by reduced or absent synthesis of the beta chains of hemoglobin that result in variable outcomes ranging from severe anemia to clinically asymptomatic individuals. Global annual incidence is estimated ...

What is beta thalassemia?

Beta thalassemia (β thalassemia) is a form of thalassemia caused by mutations in the HBB gene on chromosome 11, inherited in an autosomal recessive fashion. The severity of the disease depends on the nature of the mutation. Specialty: