α1-Antitrypsin deficiency
α1-Antitrypsin deficiency is a genetic disorder that affects the liver and lungs. It is also known as AAT deficiency or…
α1-Antitrypsin deficiency is a genetic disorder that affects the liver and lungs. It is also known as AAT deficiency or…
Haemochromatosis genotyping, Haemochromatosis is a genetic disorder characterized by excessive absorption of dietary iron, leading to iron overload in the
Anti-mitochondrial antibody, Anti-mitochondrial antibodies (AMA) are autoantibodies directed against components of the mitochondria, which are small structures
RDW Test, The red cell distribution width blood test measures the amount of red blood cell variation in volume and…
MCH Level, An MCH value refers to the average quantity of hemoglobin present in a single red blood cell. When…
Fructosamine Blood Test, A fructosamine blood test is a diagnostic tool used to measure a person's average blood glucose (sugar)…
Comprehensive Health Panel, A comprehensive health panel, also known as a comprehensive metabolic panel (CMP) or a comprehensive blood panel,…
Complement C3 is a protein that plays a critical role in the complement system, which is a part of the…