D2I2.

Blood

78 diseases · 14 high-burden in India

Alpha-thalassemia

Alpha-thalassemia is an inherited blood disorder and a form of thalassemia. Thalassemias…

Beta-thalassemia

Beta-thalassemia (β-thalassemia) is an inherited blood disorder, a form of thalassemia…

Folate-deficiency anaemia

Folate deficiency, also known as vitamin B9 deficiency, is a low level of folate and…

G6PD deficiency

Glucose-6-phosphate dehydrogenase deficiency (G6PDD), also known as favism, is the most…

Haemoglobin E disease

Hemoglobin E (HbE) is an abnormal hemoglobin with a single point mutation in the β chain.…

Hemoglobin D disease

Hemoglobin D (HbD) is a variant of hemoglobin, a protein complex that makes up red blood…

Iron-deficiency anaemia

Iron-deficiency anemia is anemia caused by a lack of iron. Anemia is defined as a…

Megaloblastic anaemia

Megaloblastic anemia is a type of macrocytic anemia. An anemia is a red blood cell defect…

Neonatal jaundice

Neonatal jaundice, clinically known as neonatal hyperbilirubinemia and icterus…

Sickle cell disease

Sickle cell disease (SCD), also simply called sickle cell, or sickle cell anemia is a…

Sickle cell trait

Sickle cell trait describes a condition in which a person has one abnormal allele of the…

Thalassaemia

Thalassemias are a group of inherited blood disorders that manifest as the production of…

Vitamin B12 deficiency

Vitamin B12 deficiency, also known as cobalamin deficiency, is the medical condition in…

Zinc deficiency

Zinc deficiency is defined either as insufficient body levels of zinc to meet the needs…

Acute lymphoblastic leukaemia

Acute lymphoblastic leukemia (ALL) is a cancer of the lymphoid line of blood cells…

Acute myeloid leukaemia

Acute myeloid leukemia (AML) is a cancer of the myeloid line of blood cells,…

Acute promyelocytic leukaemia

Acute promyelocytic leukemia is a subtype of acute myeloid leukemia (AML), a cancer of…

Agranulocytosis

Agranulocytosis, also known as agranulosis or granulopenia, is an acute condition…

Antiphospholipid syndrome

Antiphospholipid syndrome, or antiphospholipid antibody syndrome, is an autoimmune,…

Antithrombin III deficiency

Antithrombin III deficiency is a deficiency of antithrombin III. This deficiency may be…

Aplastic anaemia

Aplastic anemia (AA) is a severe hematologic condition in which the body fails to make…

Bernard–Soulier syndrome

Bernard–Soulier syndrome (BSS) is a rare autosomal recessive bleeding disorder that is…

Burkitt lymphoma

Burkitt's lymphoma is a cancer of the lymphatic system, particularly B lymphocytes found…

Chédiak–Higashi syndrome

Chédiak–Higashi syndrome (CHS) is a rare autosomal recessive disorder that arises from a…

Chronic lymphocytic leukaemia

Chronic lymphocytic leukemia (CLL) is a type of cancer that affects the blood and bone…

Chronic myeloid leukaemia

Chronic myelogenous leukemia (CML), also known as chronic myeloid leukemia, is a cancer…

Cold agglutinin disease

Cold agglutinin disease (CAD) is a rare autoimmune disease characterized by the presence…

Congenital amegakaryocytic thrombocytopenia

Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare autosomal recessive bone…

Congenital dyserythropoietic anaemia

Congenital dyserythropoietic anemia (CDA) is an umbrella term used to denote a group of…

Cryoglobulinaemia

Cryoglobulinemia is a rare medical condition characterized by the presence of…

Diamond–Blackfan anaemia

Diamond–Blackfan anemia (DBA) is a congenital pure red blood cell aplasia that usually…

Disseminated intravascular coagulation

Disseminated intravascular coagulation (DIC) is a condition in which blood clots form…

Dyskeratosis congenita

Dyskeratosis congenita (DKC), also known as Zinsser-Engman-Cole syndrome, is a rare…

Eosinophilia

Eosinophilia is a condition in which the eosinophil count in the peripheral blood exceeds…

Essential thrombocythaemia

In hematology, essential thrombocythemia (ET) is a rare chronic blood cancer…

Factor V Leiden

Factor V Leiden is a variant of human factor V, which causes an increase in blood…

Fanconi anaemia

Fanconi anemia (FA), also known as Fanconi cancer, is a rare, autosomal recessive genetic…

Felty's syndrome

Felty's syndrome (FS), also called Felty syndrome, is a rare autoimmune disease…

Gaucher disease

Gaucher's disease or Gaucher disease (GD) is a genetic disorder in which glucocerebroside…

Glanzmann's thrombasthenia

Glanzmann's thrombasthenia is an abnormality of the platelets. It is an extremely rare…

Gray platelet syndrome

Gray platelet syndrome (GPS), or platelet alpha-granule deficiency, is a rare congenital…

Haemoglobin C disease

Hemoglobin C is an abnormal hemoglobin in which glutamic acid residue at the 6th position…

Haemoglobin SC disease

Hemoglobin C is an abnormal hemoglobin in which glutamic acid residue at the 6th position…

Haemolytic anaemia

Hemolytic anemia or haemolytic anaemia is a form of anemia due to hemolysis, the abnormal…

Haemophagocytic lymphohistiocytosis

In hematology, hemophagocytic lymphohistiocytosis (HLH), also known as haemophagocytic…

Haemophilia

Haemophilia, or hemophilia, is a mostly inherited genetic disorder that impairs the…

Hairy cell leukaemia

Hairy cell leukemia is an uncommon hematological malignancy characterized by an…

Heparin-induced thrombocytopenia

Heparin-induced thrombocytopenia (HIT) is the development of thrombocytopenia, due to the…

Hereditary elliptocytosis

Hereditary elliptocytosis, also known as ovalocytosis, is an inherited blood disorder in…

Hereditary spherocytosis

Hereditary spherocytosis (HS) is a congenital hemolytic disorder wherein a genetic…

Hodgkin lymphoma

Hodgkin lymphoma (HL) is a cancer where multinucleated Reed–Sternberg cells are present…

Immune thrombocytopenia

Immune thrombocytopenic purpura (ITP), also known as idiopathic thrombocytopenic purpura…

Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is an abnormal clonal proliferation of Langerhans…

Leukaemia

Leukemia is a group of blood cancers that usually begin in the bone marrow and produce…

Lymphoma

Lymphoma is a group of blood and lymph tumors that develop from lymphocytes. The name…

Mastocytosis

Mastocytosis, a type of mast cell disease, is a rare disorder affecting both children and…

May–Hegglin anomaly

May–Hegglin anomaly (MHA), is a rare genetic disorder of the blood platelets that causes…

Methaemoglobinaemia

Methemoglobinemia, or methaemoglobinaemia, is a condition of elevated methemoglobin in…

MGUS

Monoclonal gammopathy of undetermined significance (MGUS) is a plasma cell dyscrasia in…

Multiple myeloma

Multiple myeloma (MM), also known as plasma cell myeloma and simply myeloma, is a cancer…

Myelodysplastic syndrome

A myelodysplastic syndrome (MDS) is one of a group of cancers in which blood cells in the…

Myelofibrosis

Primary myelofibrosis (PMF) is a rare bone marrow blood cancer. It is classified by the…

Neutropenia

Neutropenia is an abnormally low concentration of neutrophils in the blood. Neutrophils…

Non-Hodgkin lymphoma

Non-Hodgkin lymphoma (NHL), also known as non-Hodgkin's lymphoma, is a group of blood…

Paroxysmal nocturnal haemoglobinuria

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired, life-threatening disease…

Pernicious anaemia

Pernicious anemia is a disease where not enough red blood cells are produced due to a…

Polycythemia vera

In oncology, polycythemia vera (PV) is an uncommon myeloproliferative neoplasm in which…

Porphyria

Porphyria is a group of disorders in which substances called porphyrins build up in the…

Protein S deficiency

Protein S deficiency is a disorder associated with increased risk of venous thrombosis.…

Pure red cell aplasia

Pure red cell aplasia (PRCA) or erythroblastopenia is a type of aplastic anemia affecting…

Pyruvate kinase deficiency

Pyruvate kinase deficiency (PKD) is an inherited metabolic disorder of the enzyme…

Severe congenital neutropenia

Severe congenital neutropenia (SCN), also often known as Kostmann syndrome or Kostmann…

Sézary syndrome

Sézary disease, or Sézary syndrome, is a type of cutaneous T-cell lymphoma that was first…

Sideroblastic anaemia

Sideroblastic anemia, or sideroachrestic anemia, is a form of anemia in which the bone…

Thrombophilia

Thrombophilia is an abnormality of blood coagulation that increases the risk of…

Thrombotic thrombocytopenic purpura

Thrombotic thrombocytopenic purpura (TTP) is a blood disorder that results in blood clots…

Von Willebrand disease

Von Willebrand disease (VWD) is a type of blood-clotting disorder. It is the most common…

Waldenström macroglobulinaemia

Waldenström macroglobulinemia is a type of cancer affecting two types of white blood…

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