Category: Database: Disease
Heparin-Induced Thrombocytopenia
Heparin-Induced Thrombocytopenia (HIT) is a serious, immune-mediated complication of heparin therapy characterized by a paradoxical association of low platelet counts…
Lutetium (Lu)
Lutetium (Lu) is a dense, silvery-white, and hard rare earth metal with atomic number 71, occupying the final position in…
Haemophilia B
Haemophilia B, also known as Christmas disease, is a genetic bleeding disorder caused by deficiency in clotting factor IX (FIX)….
Haemophilia A
Haemophilia A is a genetic bleeding disorder caused by a deficiency in clotting factor VIII (FVIII). This X-linked recessive condition…
Antithrombin III Deficiency
Antithrombin III (ATIII) deficiency is a rare inherited or acquired thrombophilic disorder characterized by reduced levels or impaired function of…
Protein S Deficiency
Protein S deficiency is an inherited or acquired thrombophilic disorder characterized by decreased levels or impaired function of protein S,…
Nephrotic Syndrome
Nephrotic Syndrome is a collection of symptoms that occur when the kidneys’ filtering units (glomeruli) are damaged, leading to excessive…
Myeloproliferative Neoplasm
Myeloproliferative Neoplasms (MPNs) are a group of chronic blood cancers characterized by the abnormal proliferation of one or more types…
Paroxysmal Nocturnal Hemoglobinuria
Paroxysmal Nocturnal Hemoglobinuria (PNH) is a rare acquired blood disorder characterized by the destruction of red blood cells (hemolysis), blood…
Antiphospholipid Syndrome
Antiphospholipid Syndrome (APS) is an autoimmune disorder where the immune system mistakenly creates antibodies against certain phospholipids, which are normal…
Protein C Deficiency
Protein C deficiency is an inherited or acquired thrombophilic disorder characterized by decreased levels or impaired function of protein C,…
Disseminated Intravascular Coagulation
Disseminated Intravascular Coagulation (DIC) is a serious condition characterized by simultaneous widespread blood clotting and bleeding throughout the body. This…
Haemophilia
Haemophilia is a rare genetic bleeding disorder that impairs the body’s ability to form blood clots properly. This condition primarily…
Afibrinogenemia
Afibrinogenemia is a rare inherited blood disorder characterized by the complete absence or extremely low levels of fibrinogen (also known…
Thrombotic Thrombocytopenic Purpura
Thrombotic thrombocytopenic purpura (TTP) is a rare but life-threatening thrombotic microangiopathy characterized by widespread formation of platelet-rich clots (microthrombi) in…