icd 9 code for thalassemia major

What is the ICD 10 code for thalassemia?

282.40 is a legacy non-billable code used to specify a medical diagnosis of thalassemia, unspecified. This code was replaced on September 30, 2015 by its ICD-10 equivalent. References found for the code 282.40 in the Index of Diseases and Injuries:

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 hemolytic anemia?

This is the American ICD-10-CM version of D56.9 - other international versions of ICD-10 D56.9 may differ. A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains.

What is the ICD 9 code for Thalassemia?

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

How is Thalassemia major 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.

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.

What is the code for severe alpha thalassemia?

ICD-10-CM Code for Alpha thalassemia D56. 0.

What is thalassemia major?

This condition is called thalassemia major, or Cooley anemia. Babies born with two defective beta hemoglobin genes usually are healthy at birth but develop signs and symptoms within the first two years of life. A milder form, called thalassemia intermedia, also can result from two mutated genes.

What is thalassemia major and minor?

A person who has thalassemia trait may not have any symptoms at all or may have only mild anemia, while a person with thalassemia major may have severe symptoms and may need regular blood transfusions.

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 the ICD-10 code for alpha thalassemia carrier in pregnancy?

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.

What is beta thalassemia?

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 homozygous alpha thalassemia?

Homozygous alpha-thalassemia. Lack of all four alpha globin genes is associated with a severe intrauterine hemolytic anemia and hydrops fetalis, with massive hepatosplenomegaly, and, in most instances, fetal demise. The RBCs are very hypochromic, fragmented, and bizarre in shape.

What is the cause of alpha thalassemia?

Alpha thalassemia is caused by mutations in two different genes, the HBA1 and the HBA2 genes. Most individuals inherit two copies of each gene (for a total of four genes); one of each from a person's father, and one of each gene from a person's mother.

What is heterozygous thalassemia?

Heterozygous beta thalassemia minor (HBT) is a benign blood disorder caused by a hereditary reduction in beta globin synthesis, which often leads to mild anemia and is characterized by hypochromic microcytic erythrocyte indexes [1].

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 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.

What is the term for a group of hereditary hemolytic anemias that have in common a decreased

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.

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.