ICD-10-CM Code for Pure hypercholesterolemia, unspecified E78. 00.
Valid for SubmissionICD-10:Z83.42Short Description:Family history of familial hypercholesterolemiaLong Description:Family history of familial hypercholesterolemia
Z83.42E78. 01: Familial hypercholesterolemia. Z83. 42: Family history of familial hypercholesterolemia.Jul 1, 2016
Other hyperlipidemiaICD-10 | Other hyperlipidemia (E78. 49)
high blood cholesterol levelHypercholesterolemia is the term used to refer to a high blood cholesterol level. Cholesterol is a waxy substance that is produced by the liver and is a component of all cells found in the body.Feb 26, 2019
Hyperlipidemia is an umbrella term that includes various disorders that cause high lipid levels in the blood. Hypercholesterolemia is a type of hyperlipidemia that involves above normal levels of cholesterol in the blood.
What is familial hypercholesterolaemia (FH)? FH is an inherited condition that is passed down through families and is caused by one or more faulty genes. It's caused by a genetic mutation that means your liver is unable to remove excess 'bad' cholesterol, known as LDL.
E66Code E66* is the diagnosis code used for Overweight and Obesity. It is a disorder marked by an abnormally high, unhealthy amount of body fat.
Code I25* is the diagnosis code used for Chronic Ischemic Heart Disease, also known as Coronary artery disease (CAD).
2022 ICD-10-CM Diagnosis Code E78. 5: Hyperlipidemia, unspecified.
ICD-Code R07. 9 is a billable ICD-10 code used for healthcare diagnosis reimbursement of Chest Pain, Unspecified.
E66.01E66. 01 is morbid (severe) obesity from excess calories.Jun 25, 2017
Clinical Information. A group of familial disorders characterized by elevated circulating cholesterol contained in either low-density lipoproteins alone or also in very-low-density lipoproteins (pre-beta lipoproteins).
Characterized by increased plasma concentration of cholesterol carried in low density lipoproteins (ldl) and by a deficiency in a cell surface receptor which regulates ldl degradation and cholesterol synthesis. Hypercholesterolemia that is caused by mutation in the low density lipoprotein receptor gene.
Familial hypercholesterolemia (abbreviated FH, also spelled familial hypercholesterolaemia) is a genetic disorder characterized by high cholesterol levels, specifically very high levels of low-density lipoprotein (LDL, "bad cholesterol"), in the blood and early cardiovascular disease. Since individuals with FH underlying body biochemistry is slightly different, their high cholesterol levels are less responsive to the kinds of cholesterol control methods which are usually more effective in people without FH (such as dietary modification and statin tablets). Nevertheless, treatment (including higher statin doses) is usually effective.
Since individuals with FH underlying body biochemistry is slightly different, their high cholesterol levels are less responsive to the kinds of cholesterol control methods which are usually more effective in people without FH (such as dietary modification and statin tablets).