78 diseases · 14 high-burden in India
Alpha-thalassemia is an inherited blood disorder and a form of thalassemia. Thalassemias…
Beta-thalassemia (β-thalassemia) is an inherited blood disorder, a form of thalassemia…
Folate deficiency, also known as vitamin B9 deficiency, is a low level of folate and…
Glucose-6-phosphate dehydrogenase deficiency (G6PDD), also known as favism, is the most…
Hemoglobin E (HbE) is an abnormal hemoglobin with a single point mutation in the β chain.…
Hemoglobin D (HbD) is a variant of hemoglobin, a protein complex that makes up red blood…
Iron-deficiency anemia is anemia caused by a lack of iron. Anemia is defined as a…
Megaloblastic anemia is a type of macrocytic anemia. An anemia is a red blood cell defect…
Neonatal jaundice, clinically known as neonatal hyperbilirubinemia and icterus…
Sickle cell disease (SCD), also simply called sickle cell, or sickle cell anemia is a…
Sickle cell trait describes a condition in which a person has one abnormal allele of the…
Thalassemias are a group of inherited blood disorders that manifest as the production of…
Vitamin B12 deficiency, also known as cobalamin deficiency, is the medical condition in…
Zinc deficiency is defined either as insufficient body levels of zinc to meet the needs…
Acute lymphoblastic leukemia (ALL) is a cancer of the lymphoid line of blood cells…
Acute myeloid leukemia (AML) is a cancer of the myeloid line of blood cells,…
Acute promyelocytic leukemia is a subtype of acute myeloid leukemia (AML), a cancer of…
Agranulocytosis, also known as agranulosis or granulopenia, is an acute condition…
Antiphospholipid syndrome, or antiphospholipid antibody syndrome, is an autoimmune,…
Antithrombin III deficiency is a deficiency of antithrombin III. This deficiency may be…
Aplastic anemia (AA) is a severe hematologic condition in which the body fails to make…
Bernard–Soulier syndrome (BSS) is a rare autosomal recessive bleeding disorder that is…
Burkitt's lymphoma is a cancer of the lymphatic system, particularly B lymphocytes found…
Chédiak–Higashi syndrome (CHS) is a rare autosomal recessive disorder that arises from a…
Chronic lymphocytic leukemia (CLL) is a type of cancer that affects the blood and bone…
Chronic myelogenous leukemia (CML), also known as chronic myeloid leukemia, is a cancer…
Cold agglutinin disease (CAD) is a rare autoimmune disease characterized by the presence…
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare autosomal recessive bone…
Congenital dyserythropoietic anemia (CDA) is an umbrella term used to denote a group of…
Cryoglobulinemia is a rare medical condition characterized by the presence of…
Diamond–Blackfan anemia (DBA) is a congenital pure red blood cell aplasia that usually…
Disseminated intravascular coagulation (DIC) is a condition in which blood clots form…
Dyskeratosis congenita (DKC), also known as Zinsser-Engman-Cole syndrome, is a rare…
Eosinophilia is a condition in which the eosinophil count in the peripheral blood exceeds…
In hematology, essential thrombocythemia (ET) is a rare chronic blood cancer…
Factor V Leiden is a variant of human factor V, which causes an increase in blood…
Fanconi anemia (FA), also known as Fanconi cancer, is a rare, autosomal recessive genetic…
Felty's syndrome (FS), also called Felty syndrome, is a rare autoimmune disease…
Gaucher's disease or Gaucher disease (GD) is a genetic disorder in which glucocerebroside…
Glanzmann's thrombasthenia is an abnormality of the platelets. It is an extremely rare…
Gray platelet syndrome (GPS), or platelet alpha-granule deficiency, is a rare congenital…
Hemoglobin C is an abnormal hemoglobin in which glutamic acid residue at the 6th position…
Hemoglobin C is an abnormal hemoglobin in which glutamic acid residue at the 6th position…
Hemolytic anemia or haemolytic anaemia is a form of anemia due to hemolysis, the abnormal…
In hematology, hemophagocytic lymphohistiocytosis (HLH), also known as haemophagocytic…
Haemophilia, or hemophilia, is a mostly inherited genetic disorder that impairs the…
Hairy cell leukemia is an uncommon hematological malignancy characterized by an…
Heparin-induced thrombocytopenia (HIT) is the development of thrombocytopenia, due to the…
Hereditary elliptocytosis, also known as ovalocytosis, is an inherited blood disorder in…
Hereditary spherocytosis (HS) is a congenital hemolytic disorder wherein a genetic…
Hodgkin lymphoma (HL) is a cancer where multinucleated Reed–Sternberg cells are present…
Immune thrombocytopenic purpura (ITP), also known as idiopathic thrombocytopenic purpura…
Langerhans cell histiocytosis (LCH) is an abnormal clonal proliferation of Langerhans…
Leukemia is a group of blood cancers that usually begin in the bone marrow and produce…
Lymphoma is a group of blood and lymph tumors that develop from lymphocytes. The name…
Mastocytosis, a type of mast cell disease, is a rare disorder affecting both children and…
May–Hegglin anomaly (MHA), is a rare genetic disorder of the blood platelets that causes…
Methemoglobinemia, or methaemoglobinaemia, is a condition of elevated methemoglobin in…
Monoclonal gammopathy of undetermined significance (MGUS) is a plasma cell dyscrasia in…
Multiple myeloma (MM), also known as plasma cell myeloma and simply myeloma, is a cancer…
A myelodysplastic syndrome (MDS) is one of a group of cancers in which blood cells in the…
Primary myelofibrosis (PMF) is a rare bone marrow blood cancer. It is classified by the…
Neutropenia is an abnormally low concentration of neutrophils in the blood. Neutrophils…
Non-Hodgkin lymphoma (NHL), also known as non-Hodgkin's lymphoma, is a group of blood…
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired, life-threatening disease…
Pernicious anemia is a disease where not enough red blood cells are produced due to a…
In oncology, polycythemia vera (PV) is an uncommon myeloproliferative neoplasm in which…
Porphyria is a group of disorders in which substances called porphyrins build up in the…
Protein S deficiency is a disorder associated with increased risk of venous thrombosis.…
Pure red cell aplasia (PRCA) or erythroblastopenia is a type of aplastic anemia affecting…
Pyruvate kinase deficiency (PKD) is an inherited metabolic disorder of the enzyme…
Severe congenital neutropenia (SCN), also often known as Kostmann syndrome or Kostmann…
Sézary disease, or Sézary syndrome, is a type of cutaneous T-cell lymphoma that was first…
Sideroblastic anemia, or sideroachrestic anemia, is a form of anemia in which the bone…
Thrombophilia is an abnormality of blood coagulation that increases the risk of…
Thrombotic thrombocytopenic purpura (TTP) is a blood disorder that results in blood clots…
Von Willebrand disease (VWD) is a type of blood-clotting disorder. It is the most common…
Waldenström macroglobulinemia is a type of cancer affecting two types of white blood…