icd 10 code for beta thalassemia minor

What is β thalassemia minor?

Beta thalassemia minor or thalassemia trait. Only one gene is damaged. This causes less severe anemia. People with this type have a 50% chance of passing the gene to their children. If the other parent is not affected, their children will also have this form of the disorder.

What is the ICD 10 code for thalassemia minor?

D56. 3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

Is thalassemia minor the same as beta?

Beta thalassemia trait is also known as beta thalassemia minor. If one parent has beta thalassemia trait and the other parent has normal hemoglobin A, there is a 50 percent (1 in 2) chance with each pregnancy of having a child with beta thalassemia trait. These are the possible outcomes with each pregnancy.

What is thalassemia major and minor?

If you inherit: 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.Nov 17, 2021

How do you know if you have thalassemia minor?

Abnormally shaped red blood cells are a sign of thalassemia. The lab technician may also perform a test known as hemoglobin electrophoresis. This test separates out the different molecules in the red blood cells, allowing them to identify the abnormal type.

Is thalassemia trait the same as thalassemia minor?

People who have thalassemia trait (also called thalassemia minor) carry the genetic trait for thalassemia but do not usually experience any health problems except perhaps a mild anemia. A person may have either alpha thalassemia trait or beta thalassemia trait, depending upon which form of beta protein is lacking.

What is beta plus thalassemia?

Sickle beta plus thalassemia (HbS β+thal) is a mild form of sickle cell disease. Many babies with HbS β+thal are born healthy and do not show symptoms until later in childhood. Some problems can include low red blood cell count, pain, and risk of infection.

What is the difference between alpha 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 beta thalassemia?

BETA THALASSEMIA-. a disorder characterized by reduced synthesis of the beta chains of hemoglobin. 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 a type 1 exclude note?

Type 1 Excludes. 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.

What is the most common type of anemia?

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.

What is the blood disorder that reduces the production of hemoglobin?

Alpha thalassemia Alpha thalassemia is a blood disorder that reduces the production of hemoglobin. Hemoglobin is the protein in red blood cells that carries oxygen to cells throughout the body.In people with the characteristic features of alpha thalassemia, a reduction in the amount of hemoglobin prevents enough oxygen from reaching ...

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 thalassemia caused by?

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.

What is inclusion term?

Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.