icd 9 code for beta thalassemia intermedia

Full Answer

What is the ICD 9 code for thalassemia?

Thalassemia (disease) 282.40. beta (homozygous) (major) (severe) 282.44. intermedia 282.44. major 282.44. 282.43. ICD9Data.com. 282.45. ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 282.44 is one of thousands of ICD-9-CM codes used in healthcare.

What are the ICD-9 codes for erythroblastic anemia?

Cooley's (erythroblastic anemia) 282.44 Thalassemia (disease) 282.40 beta (homozygous) (major) (severe) 282.44 intermedia 282.44 major 282.44 282.43 ICD9Data.com 282.45 ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions.

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

Cooley's anemia (erythroblastic) 282.44 Disease, diseased - see also Syndrome Cooley's (erythroblastic anemia) 282.44 Thalassemia (disease) 282.40 beta (homozygous) (major) (severe) 282.44 intermedia 282.44 major 282.44 282.43 ICD9Data.com 282.45

What is the ICD-9-CM Diagnosis Code for hemolytic anemia?

Free, official information about 2012 (and also 2013-2015) ICD-9-CM diagnosis code 282.44, including coding notes, detailed descriptions, index cross-references and ICD-10-CM conversion. Home> 2012 ICD-9-CM Diagnosis Codes> Diseases Of The Blood And Blood-Forming Organs 280-289> Hereditary hemolytic anemias 282-

What is beta thalassemia intermedia?

β-Thalassemia intermedia is a clinical condition of intermediate gravity between β-thalassemia minor, the asymptomatic carrier, and β-thalassemia major, the transfusion-dependent severe anemia. It is characterized by a significant clinical polymorphism, which is attributable to its genetic heterogeneity.

What is thalassemia major and intermedia?

Individuals with beta thalassemia major require regular blood transfusions, as frequently as every 2-4 weeks in severe cases. Individuals with beta thalassemia intermedia occasionally require blood transfusions such as when suffering from an illness or infection or when planning to undergo surgery.

What is the difference between thalassemia minor and Intermedia?

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.

Is thalassemia a homozygous Intermedia?

Thalassemia intermedia is characterized by a significant genetic and clinical heterogeneity. A wide spectrum of different genotypes – homozygous, heterozygous and compound heterozygous – have been thought to be responsible for thalassemia intermedia.

Is beta thalassemia intermedia heterozygous?

Thalassemia intermedia: compound heterozygous beta zero/beta(+)-thalassemia and co-inherited heterozygous alpha(+)-thalassemia. Ann Hematol.

How is beta thalassemia intermedia diagnosed?

Diagnosis is confirmed by a hemoglobin profile (also called electrophoresis). In beta thalassemia intermedia and trait, this testing reveals an elevation in hemoglobin A2 (a second form of adult hemoglobin) and sometimes F (fetal).

Can thalassemia minor turn into Intermedia?

Thalassemia intermedia is a clinical designation for syndromes in which the α/β chain imbalance and symptoms fall between those observed in β-thalassemia minor and β-thalassemia major, but without the need for regular transfusion therapy to maintain the hemoglobin level and quality of life.

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 types of beta thalassemia?

The three main types of beta thalassemia (BAY-tuh thahl-uh-SEE-mee-uh) are:Beta thalassemia trait (also called beta thalassemia minor). ... Beta thalassemia intermedia. ... Beta thalassemia major (also called Cooley's anemia).

What is beta thalassemia intermedia genotype?

The clinical syndrome of thalassemia intermedia (TI) results from the β-globin genotypes in combination with factors to produce fetal haemoglobin (HbF) and/or co-inheritance of α-thalassemia.

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 is the difference between thalassemia alpha and beta?

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 the ICd 10 code for thalassemia?

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.

How to diagnose thalassemia?

Doctors diagnose thalassemias using blood tests. Treatments include blood transfusions and treatment to remove excess iron from the body. If you have mild symptoms or no symptoms, you may not need treatment. In some severe cases, you may need a bone marrow transplant.

What is a type 1 exclude note?

Type 1 Excludes Notes - A type 1 Excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.

What is a code also note?

Code also note - A "code also" note instructs that two codes may be required to fully describe a condition, but this note does not provide sequencing direction.

Is thalassemia mild or severe?

Thalassemias can be mild or severe. Some people have no symptoms or mild anemia. The most common severe type in the United States is called Cooley's anemia. It usually appears during the first two years of life. People with it may have severe anemia, slowed growth and delayed puberty, and problems with the spleen, liver, heart, or bones.

When will the ICd 10 D56.1 be released?

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

Is thalassemia asymptomatic or heterozygous?

There is retardation of hemoglobin a synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, cooley's anemia, mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin a synthesis is absent.

What is the ICD code for beta thalassemia?

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.

What is thalassemia in blood?

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 at 1 in 100,000. 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.