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The following 72,752 ICD-10-CM codes are billable/specific and can be used to indicate a diagnosis for reimbursement purposes as there are no codes with a greater level of specificity under each code. Displaying codes 1-100 of 72,752: A00.0 Cholera due to Vibrio cholerae 01, biovar cholerae. A00.1 Cholera due to Vibrio cholerae 01, biovar eltor. A00.9 Cholera, unspecified.
The ICD-10-CM is a catalog of diagnosis codes used by medical professionals for medical coding and reporting in health care settings. The Centers for Medicare and Medicaid Services (CMS) maintain the catalog in the U.S. releasing yearly updates.
V78. 2 - Screening for sickle-cell disease or trait | ICD-10-CM.
Hemoglobin SS disease is the most common and most severe type of sickle cell disease. It occurs when you inherit the hemoglobin S gene mutation from both parents. In this type, the body only produces hemoglobin S. This type is often called “sickle cell anemia.”
Overview. Sickle beta thalassemia is an inherited condition that affects hemoglobin, the protein in red blood cells that carries oxygen to different parts of the body. It is a type of sickle cell disease.
ICD-10 | Fever, unspecified (R50. 9)
Blood genotype indicates of the type of protein (Haemoglobin) that is in the red blood cells. You could be Haemoglobin AA, AS, AC, SS or SC based on what is inherited from your parents. Individuals with blood genotype SC and SS are said to have sickle cell disease while AS is known as sickle cell trait.
The four main types of sickle cell anemia are caused by different mutations in these genes.Hemoglobin SS disease. ... Hemoglobin SC disease. ... Hemoglobin SB+ (beta) thalassemia. ... Hemoglobin SB 0 (Beta-zero) thalassemia. ... Hemoglobin SD, hemoglobin SE, and hemoglobin SO. ... Sickle cell trait.
While beta thalassemia is caused by a defect in the beta-globin gene, controlling the production of the beta-globin chains of hemoglobin, sickle cell disease is caused by a defect in hemoglobin itself with the presence of abnormal hemoglobin S.
Anemia is a condition in which your body doesn't have enough normal, healthy red blood cells. Thalassemia is inherited, meaning that at least one of your parents must be a carrier of the disorder. It's caused by either a genetic mutation or a deletion of certain key gene fragments.
In sickle cell anemia (also called homozygous sickle cell disease), which is the most common form of sickle cell disease, hemoglobin S replaces both beta-globin subunits in hemoglobin.
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.
ICD-9 Code Transition: 780.79 Code R53. 83 is the diagnosis code used for Other Fatigue. It is a condition marked by drowsiness and an unusual lack of energy and mental alertness. It can be caused by many things, including illness, injury, or drugs.
ICD-10 code R51 for Headache is a medical classification as listed by WHO under the range - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified .
If you only have one sickle cell gene, it's called sickle cell trait . About 1 in 12 african americans has sickle cell trait . A blood test can show if you have the trait or anemia. Most states test newborn babies as part of their newborn screening programs.
A blood disorder characterized by the appearance of sickle-shaped red blood cells and anemia. A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin s.
Sickle cell anemia is caused by a mutation (change) in one of the genes for hemoglobin (the substance inside red blood cells that binds to oxygen and carries it from the lungs to the tissues). It is most common in people of west and central african descent.
The sickle cells also get stuck in blood vessels, blocking blood flow. This can cause pain and organ damage. A genetic problem causes sickle cell anemia. People with the disease are born with two sickle cell genes, one from each parent. If you only have one sickle cell gene, it's called sickle cell trait.
A blood disorder characterized by the appearance of sickle-shaped red blood cells and anemia. A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin s.
Sickle cell anemia is caused by a mutation (change) in one of the genes for hemoglobin (the substance inside red blood cells that binds to oxygen and carries it from the lungs to the tissues). It is most common in people of west and central african descent.
The sickle cells also get stuck in blood vessels, blocking blood flow. This can cause pain and organ damage. A genetic problem causes sickle cell anemia. People with the disease are born with two sickle cell genes, one from each parent. If you only have one sickle cell gene, it's called sickle cell trait.