icd 10 code for beta thalassemia

Beta thalassemia. D56.1 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 D56.1 became effective on October 1, 2018.

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What is the ICD 10 code for thalassemia?

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

What is the ICD 10 code for Cooley's anemia?

Beta thalassemia (D56.1) D56.0 D56.1 D56.2 ICD-10-CM Code for Beta thalassemia D56.1 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 . Subscribe to Codify and get the code details in a flash.

What is the ICD 10 code for Mediterranean anemia?

Beta thalassemia BILLABLE | ICD-10 from 2011 - 2016 D56.1 is a billable ICD code used to specify a diagnosis of beta thalassemia. A 'billable code' is detailed enough to be used to specify a medical diagnosis. The ICD code D561 is used to code Beta thalassemia Beta thalassemias (β thalassemias) are a group of inherited blood disorders.

What is the ICD 10 code for hemolytic anemia?

Oct 01, 2021 · D56.1. Beta thalassemia Billable Code. D56.1 is a valid billable ICD-10 diagnosis code for Beta 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 thalassemia trait?

ICD-10-CM Code for Thalassemia minor D56. 3.

What is beta thalassemia?

Beta thalassemia is a blood disorder that reduces the production of hemoglobin . Hemoglobin is the iron-containing protein in red blood cells that carries oxygen to cells throughout the body. In people with beta thalassemia, low levels of hemoglobin lead to a lack of oxygen in many parts of the body.

What are the 4 types of beta thalassemia?

There are several types of this disorder:Beta thalassemia major (Cooley's anemia). ... Beta thalassemia minor or thalassemia trait. ... Beta thalassemia major: This is the most severe type of this disorder. ... Thalassemia minima: This type often causes no symptoms.More items...

Is there another name for beta thalassemia?

Beta thalassemia major (also called Cooley's anemia). People with beta thalassemia major have life-threatening anemia. They need regular blood transfusions and other medical care.

How is beta thalassemia diagnosed?

A blood sample can be tested to measure the amount of iron in the blood, which is often elevated in individuals with beta thalassemia. Molecular genetic testing can confirm a beta thalassemia diagnosis.

What is the difference between beta thalassemia major and minor?

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.

What type of mutation is beta thalassemia?

Beta thalassemia major is caused by a homozygous mutation (beta-zero thalassemia) of the beta-globin gene, resulting in the total absence of beta chains. It manifests clinically as jaundice, growth retardation, hepatosplenomegaly, endocrine abnormalities, and severe anemia requiring life-long blood transfusions.Nov 5, 2021

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 thalassemia and its types?

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.Jun 2, 2020

What is the another name of thalassemia?

ThalassemiaOther namesThalassaemia, Mediterranean anemiaPeripheral blood film from a person with delta-beta thalassemiaPronunciation/θælɪˈsiːmiə/SpecialtyHematology7 more rows

What is the pathophysiology of beta thalassemia?

β thalassemia occurs when there is a quantitative reduction of β globin chains that are usually structurally normal. They are caused by mutations that nearly all affect the β globin locus and are extremely heterogeneous.Jan 1, 2005

Is thalassemia a chromosomal disorder?

Thalassemia is an inherited autosomal recessive disease resulting from mutations in the α- and β-globin gene clusters on chromosome 16 and chromosome 11, respectively. It is characterized by the absence or reduced synthesis of globin chains of hemoglobin and includes two main types, α- and β- thalassemia (1, 2).Apr 15, 2020

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:

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.

What is hemolytic anemia?

A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.