Logo
Unionpedia
Communication
Get it on Google Play
New! Download Unionpedia on your Android™ device!
Free
Faster access than browser!
 

ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism

Index ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism

ICD-10 is an international statistical classification used in health care and related industries. [1]

176 relations: Acquired C1 esterase inhibitor deficiency, Acquired hemolytic anemia, Acute posthemorrhagic anemia, Adenosine deaminase, Adenosine deaminase deficiency, Agranulocytosis, Alpha-thalassemia, Anemia, Antibody, Aplastic anemia, Asplenia, Autoimmune hemolytic anemia, B cell, Bare lymphocyte syndrome, Basophilia, Bernard–Soulier syndrome, Beta thalassemia, Bleeding, Blood, C1-inhibitor, Chronic condition, Chronic granulomatous disease, Coagulation, Coagulopathy, Combined immunodeficiencies, Common variable immunodeficiency, Complement system, Congenital afibrinogenemia, Congenital dyserythropoietic anemia, Congenital hypoplastic anemia, Crisis, Cryoglobulinemia, Cytochrome b5 reductase, Diamond–Blackfan anemia, DiGeorge syndrome, Disseminated intravascular coagulation, Drug-induced autoimmune hemolytic anemia, Drug-induced nonautoimmune hemolytic anemia, Dysphagia, Enzyme, Eosinophilia, Eosinophilic granuloma, Epstein–Barr virus, Essential thrombocythemia, Evans syndrome, Factor IX, Factor VIII, Factor XI, Fanconi anemia, Folate deficiency, ..., Functional disorder, Glanzmann's thrombasthenia, Glucose-6-phosphate dehydrogenase, Glucose-6-phosphate dehydrogenase deficiency, Glutathione, Glycolysis, Gray platelet syndrome, Haemophilia A, Haemophilia B, Haemophilia C, Hand–Schüller–Christian disease, Health care, Hemoglobinopathy, Hemoglobinuria, Hemolysis, Hemolytic anemia, Hemolytic-uremic syndrome, Hemophagocytic lymphohistiocytosis, Henoch–Schönlein purpura, Hereditary elliptocytosis, Hereditary persistence of fetal hemoglobin, Hereditary spherocytosis, Hereditary stomatocytosis, Heredity, Hexokinase deficiency, Histiocytosis, Humoral immune deficiency, Hyper IgM syndrome, Hypergammaglobulinemia, Hyperimmunoglobulin E syndrome, Hypogammaglobulinemia, Hypoplasia, ICD-10, ICD-10 Chapter I: Certain infectious and parasitic diseases, ICD-10 Chapter II: Neoplasms, IgG deficiency, Immune system, Immune thrombocytopenic purpura, Immunodeficiency, Immunoglobulin A, Immunoglobulin E, Immunoglobulin G, Immunoglobulin M, International Statistical Classification of Diseases and Related Health Problems, Intrinsic factor, Iron deficiency, Iron-deficiency anemia, Isolated primary immunoglobulin M deficiency, Juvenile xanthogranuloma, Kostmann syndrome, Langerhans cell histiocytosis, Leukemia, Leukemoid reaction, Leukocytosis, List of ICD-9 codes 140–239: neoplasms, Lung, Lymph node, Lymphadenopathy, Lymphocyte function-associated antigen 1, Lymphocytopenia, Lymphocytosis, Major histocompatibility complex, May–Hegglin anomaly, Medical classification, Megaloblastic anemia, Methemoglobinemia, MHC class I, Microangiopathic hemolytic anemia, Monocytosis, Mononuclear phagocyte system, Multiple carboxylase deficiency, Myelophthisic anemia, Neutropenia, Neutrophil, Nezelof syndrome, Nonthrombocytopenic purpura, Nucleotide, Nutritional anemia, Paroxysmal cold hemoglobinuria, Paroxysmal nocturnal hemoglobinuria, Pelger–Huet anomaly, Plasmacytosis, Platelet, Plummer–Vinson syndrome, Polyclonal antibodies, Polycythemia, Proteinuria, Pure red cell aplasia, Purine nucleoside phosphorylase deficiency, Purpura, Purpura fulminans, Pyruvate kinase deficiency, Qualitative property, Reticular dysgenesis, Reticulohistiocytoma, Rosai–Dorfman disease, Sarcoidosis, Scurvy, Selective immunoglobulin A deficiency, Sepsis, Severe combined immunodeficiency, Sickle cell disease, Sickle cell trait, Sideroblastic anemia, Skin, Southeast Asian ovalocytosis, Spleen, Splenic infarction, Splenomegaly, Sulfhemoglobinemia, T cell, Thalassemia, Thrombocytopenia, Transcobalamin, Transient hypogammaglobulinemia of infancy, Triosephosphate isomerase deficiency, Vitamin B12, Vitamin B12 deficiency anemia, Von Willebrand disease, Warm antibody autoimmune hemolytic anemia, White blood cell, Wiskott–Aldrich syndrome, World Health Organization, X-linked agammaglobulinemia, X-linked lymphoproliferative disease, X-linked severe combined immunodeficiency. Expand index (126 more) »

Acquired C1 esterase inhibitor deficiency

Acquired C1 esterase inhibitor deficiency also known as "Acquired Angioedema" presents with symptoms indistinguishable from hereditary angioedema, but generally with onset after the fourth decade of life.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Acquired C1 esterase inhibitor deficiency · See more »

Acquired hemolytic anemia

Acquired hemolytic anemia can be divided into immune and non-immune mediated forms of hemolytic anemia.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Acquired hemolytic anemia · See more »

Acute posthemorrhagic anemia

Acute posthemorrhagic anemia or acute blood loss anemia is a condition in which a person quickly loses a large volume of circulating hemoglobin.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Acute posthemorrhagic anemia · See more »

Adenosine deaminase

Adenosine deaminase (also known as adenosine aminohydrolase, or ADA) is an enzyme involved in purine metabolism.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Adenosine deaminase · See more »

Adenosine deaminase deficiency

Adenosine deaminase deficiency (also called ADA deficiency or ADA-SCID) is an autosomal recessive metabolic disorder that causes immunodeficiency.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Adenosine deaminase deficiency · See more »

Agranulocytosis

Agranulocytosis, also known as agranulosis or granulopenia, is an acute condition involving a severe and dangerous leukopenia (lowered white blood cell count), most commonly of neutrophils causing a neutropenia in the circulating blood.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Agranulocytosis · See more »

Alpha-thalassemia

Alpha-thalassemia (α-thalassemia, α-thalassaemia) is a form of thalassemia involving the genes HBA1 and HBA2.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Alpha-thalassemia · See more »

Anemia

Anemia is a decrease in the total amount of red blood cells (RBCs) or hemoglobin in the blood, or a lowered ability of the blood to carry oxygen.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Anemia · See more »

Antibody

An antibody (Ab), also known as an immunoglobulin (Ig), is a large, Y-shaped protein produced mainly by plasma cells that is used by the immune system to neutralize pathogens such as pathogenic bacteria and viruses.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Antibody · See more »

Aplastic anemia

Aplastic anaemia is a rare disease in which the bone marrow and the hematopoietic stem cells that reside there are damaged.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Aplastic anemia · See more »

Asplenia

Asplenia refers to the absence of normal spleen function and is associated with some serious infection risks.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Asplenia · See more »

Autoimmune hemolytic anemia

Autoimmune hemolytic anemia (or autoimmune haemolytic anaemia; AIHA) occurs when antibodies directed against the person's own red blood cells (RBCs) cause them to burst (lyse), leading to an insufficient number of oxygen-carrying red blood cells in the circulation.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Autoimmune hemolytic anemia · See more »

B cell

B cells, also known as B lymphocytes, are a type of white blood cell of the lymphocyte subtype.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and B cell · See more »

Bare lymphocyte syndrome

Bare lymphocyte syndrome is a condition caused by mutations in certain genes of the major histocompatibility complex or involved with the processing and presentation of MHC molecules.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Bare lymphocyte syndrome · See more »

Basophilia

Basophilia is a condition derived from Basophils.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Basophilia · See more »

Bernard–Soulier syndrome

Bernard–Soulier syndrome (BSS), also called hemorrhagiparous thrombocytic dystrophy, is a rare autosomal recessive bleeding disorder that causes a deficiency of glycoprotein Ib (GpIb), the receptor for von Willebrand factor.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Bernard–Soulier syndrome · See more »

Beta thalassemia

Beta thalassemias (β thalassemias) are a group of inherited blood disorders.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Beta thalassemia · See more »

Bleeding

Bleeding, also known as hemorrhaging or haemorrhaging, is blood escaping from the circulatory system.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Bleeding · See more »

Blood

Blood is a body fluid in humans and other animals that delivers necessary substances such as nutrients and oxygen to the cells and transports metabolic waste products away from those same cells.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Blood · See more »

C1-inhibitor

C1-inhibitor (C1-inh, C1 esterase inhibitor) is a protease inhibitor belonging to the serpin superfamily.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and C1-inhibitor · See more »

Chronic condition

A chronic condition is a human health condition or disease that is persistent or otherwise long-lasting in its effects or a disease that comes with time.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Chronic condition · See more »

Chronic granulomatous disease

Chronic granulomatous disease (CGD) (also known as Bridges–Good syndrome, chronic granulomatous disorder, and Quie syndrome) is a diverse group of hereditary diseases in which certain cells of the immune system have difficulty forming the reactive oxygen compounds (most importantly the superoxide radical due to defective phagocyte NADPH oxidase) used to kill certain ingested pathogens.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Chronic granulomatous disease · See more »

Coagulation

Coagulation (also known as clotting) is the process by which blood changes from a liquid to a gel, forming a blood clot.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Coagulation · See more »

Coagulopathy

A bleeding disorder (coagulopathy) is a condition that affects the way the blood clots.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Coagulopathy · See more »

Combined immunodeficiencies

Combined immunodeficiencies (or combined immunity deficiency) are immunodeficiency disorders that involve multiple components of the immune system, including both humoral immunity and cell-mediated immunity.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Combined immunodeficiencies · See more »

Common variable immunodeficiency

Common variable immunodeficiency (CVID) is an immune disorder characterized by recurrent infections and low antibody levels, specifically in immunoglobulin (Ig) types IgG, IgM and IgA.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Common variable immunodeficiency · See more »

Complement system

The complement system is a part of the immune system that enhances (complements) the ability of antibodies and phagocytic cells to clear microbes and damaged cells from an organism, promotes inflammation, and attacks the pathogen's cell membrane.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Complement system · See more »

Congenital afibrinogenemia

Congenital afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due to the lack of fibrinogen, a blood protein necessary for coagulation.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Congenital afibrinogenemia · See more »

Congenital dyserythropoietic anemia

Congenital dyserythropoietic anemia (CDA) is a rare blood disorder, similar to the thalassemias.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Congenital dyserythropoietic anemia · See more »

Congenital hypoplastic anemia

Congenital hypoplastic anemia (or constitutional aplastic anemia) is a type of aplastic anemia which is primarily due to a congenital disorder.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Congenital hypoplastic anemia · See more »

Crisis

A crisis (from the Greek κρίσις - krisis; plural: "crises"; adjectival form: "critical") is any event that is going (or is expected) to lead to an unstable and dangerous situation affecting an individual, group, community, or whole society.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Crisis · See more »

Cryoglobulinemia

Cryoglobulinemia, cryoglobulinaemia, or cryoglobulinemic disease, is a medical condition in which the blood contains large amounts of cryoglobulins – proteins (mostly immunoglobulins themselves) that become insoluble at reduced temperatures.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Cryoglobulinemia · See more »

Cytochrome b5 reductase

Cytochrome-b5 reductase (also known as methemoglobin reductase) is a NADH-dependent enzyme that converts methemoglobin to hemoglobin.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Cytochrome b5 reductase · See more »

Diamond–Blackfan anemia

Diamond–Blackfan anemia (DBA) is a congenital erythroid aplasia that usually presents in infancy.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Diamond–Blackfan anemia · See more »

DiGeorge syndrome

DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by the deletion of a small segment of chromosome 22.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and DiGeorge syndrome · See more »

Disseminated intravascular coagulation

Disseminated intravascular coagulation (DIC) is a condition in which blood clots form throughout the body, blocking small blood vessels.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Disseminated intravascular coagulation · See more »

Drug-induced autoimmune hemolytic anemia

Drug-induced autoimmune hemolytic anemia is a form of hemolytic anemia.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Drug-induced autoimmune hemolytic anemia · See more »

Drug-induced nonautoimmune hemolytic anemia

Drug-induced nonautoimmune hemolytic anemia is a form of hemolytic anemia.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Drug-induced nonautoimmune hemolytic anemia · See more »

Dysphagia

Dysphagia is the medical term for the symptom of difficulty in swallowing.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Dysphagia · See more »

Enzyme

Enzymes are macromolecular biological catalysts.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Enzyme · See more »

Eosinophilia

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

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Eosinophilia · See more »

Eosinophilic granuloma

Eosinophilic granuloma is a form of Langerhans cell histiocytosis.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Eosinophilic granuloma · See more »

Epstein–Barr virus

The Epstein–Barr virus (EBV), also called human herpesvirus 4 (HHV-4), is one of eight known human herpesvirus types in the herpes family, and is one of the most common viruses in humans.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Epstein–Barr virus · See more »

Essential thrombocythemia

Essential thrombocythemia (ET) is a rare chronic blood condition characterised by the overproduction of platelets (thrombocytes) by megakaryocytes in the bone marrow.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Essential thrombocythemia · See more »

Evans syndrome

Evans syndrome is an autoimmune disease in which an individual's immune system attacks their own red blood cells, white blood cells, and/or platelets.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Evans syndrome · See more »

Factor IX

Factor IX (or Christmas factor) is one of the serine proteases of the coagulation system; it belongs to peptidase family S1.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Factor IX · See more »

Factor VIII

Factor VIII (FVIII) is an essential blood-clotting protein, also known as anti-hemophilic factor (AHF).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Factor VIII · See more »

Factor XI

Factor XI or plasma thromboplastin antecedent is the zymogen form of factor XIa, one of the enzymes of the coagulation cascade.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Factor XI · See more »

Fanconi anemia

Fanconi anaemia (FA) is a rare genetic disease resulting in impaired response to DNA damage.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Fanconi anemia · See more »

Folate deficiency

Folate deficiency is a low level of folic acid and derivatives in the body.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Folate deficiency · See more »

Functional disorder

A functional disorder is a medical condition that impairs normal functioning of bodily processes that remains largely undetected under examination, dissection or even under a microscope.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Functional disorder · See more »

Glanzmann's thrombasthenia

Glanzmann's thrombasthenia is an abnormality of the platelets.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Glanzmann's thrombasthenia · See more »

Glucose-6-phosphate dehydrogenase

Glucose-6-phosphate dehydrogenase (G6PD or G6PDH) is a cytosolic enzyme that catalyzes the chemical reaction This enzyme participates in the pentose phosphate pathway (see image), a metabolic pathway that supplies reducing energy to cells (such as erythrocytes) by maintaining the level of the co-enzyme nicotinamide adenine dinucleotide phosphate (NADPH).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Glucose-6-phosphate dehydrogenase · See more »

Glucose-6-phosphate dehydrogenase deficiency

Glucose-6-phosphate dehydrogenase deficiency (G6PDD) is an inborn error of metabolism that predisposes to red blood cell breakdown.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Glucose-6-phosphate dehydrogenase deficiency · See more »

Glutathione

Glutathione (GSH) is an important antioxidant in plants, animals, fungi, and some bacteria and archaea.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Glutathione · See more »

Glycolysis

Glycolysis (from glycose, an older term for glucose + -lysis degradation) is the metabolic pathway that converts glucose C6H12O6, into pyruvate, CH3COCOO− + H+.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Glycolysis · See more »

Gray platelet syndrome

Gray platelet syndrome (GPS), or platelet alpha-granule deficiency, is a rare congenital autosomal recessive bleeding disorder caused by a reduction or absence of alpha-granules in blood platelets, and the release of proteins normally contained in these granules into the marrow, causing myelofibrosis.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Gray platelet syndrome · See more »

Haemophilia A

Haemophilia A (or hemophilia A) is a genetic deficiency in clotting factor VIII, which causes increased bleeding and usually affects males.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Haemophilia A · See more »

Haemophilia B

Haemophilia B is a blood clotting disorder causing easy bruising and bleeding due to an inherited mutation of the gene for factor IX, and resulting in a deficiency of factor IX. It is less common than factor VIII deficiency (haemophilia A). Haemophilia B was first recognized as a distinct disease entity in 1952. It is also known by the eponym Christmas disease, named after Stephen Christmas, the first patient described with haemophilia B. In addition, the first report of its identification was published in the Christmas edition of the British Medical Journal.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Haemophilia B · See more »

Haemophilia C

Haemophilia C (also known as plasma thromboplastin antecedent (PTA) deficiency or Rosenthal syndrome) is a mild form of haemophilia affecting both sexes, due to factor XI deficiency.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Haemophilia C · See more »

Hand–Schüller–Christian disease

Hand–Schüller–Christian disease is associated with multifocal Langerhans cell histiocytosis.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hand–Schüller–Christian disease · See more »

Health care

Health care or healthcare is the maintenance or improvement of health via the prevention, diagnosis, and treatment of disease, illness, injury, and other physical and mental impairments in human beings.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Health care · See more »

Hemoglobinopathy

Hemoglobinopathy is a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hemoglobinopathy · See more »

Hemoglobinuria

In medicine, hemoglobinuria or haemoglobinuria is a condition in which the oxygen transport protein hemoglobin is found in abnormally high concentrations in the urine.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hemoglobinuria · See more »

Hemolysis

Hemolysis or haemolysis, also known by several other names, is the rupturing (lysis) of red blood cells (erythrocytes) and the release of their contents (cytoplasm) into surrounding fluid (e.g. blood plasma).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hemolysis · See more »

Hemolytic anemia

Hemolytic anemia or haemolytic anaemia is a form of anemia due to hemolysis, the abnormal breakdown of red blood cells (RBCs), either in the blood vessels (intravascular hemolysis) or elsewhere in the human body (extravascular, but usually in the spleen).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hemolytic anemia · See more »

Hemolytic-uremic syndrome

Hemolytic-uremic syndrome (HUS) is a disease characterized by a triad of hemolytic anemia (anemia caused by destruction of red blood cells), acute kidney failure (uremia), and a low platelet count (thrombocytopenia).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hemolytic-uremic syndrome · See more »

Hemophagocytic lymphohistiocytosis

Hemophagocytic lymphohistiocytosis (HLH), also known as haemophagocytic lymphohistiocytosis (British spelling), and hemophagocytic or haemophagocytic syndrome, is an uncommon hematologic disorder seen more often in children than in adults.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hemophagocytic lymphohistiocytosis · See more »

Henoch–Schönlein purpura

Henoch–Schönlein purpura (HSP) also known as IgA vasculitis, anaphylactoid purpura, purpura rheumatica, and Schönlein–Henoch purpura, is a disease of the skin, mucous membranes, and sometimes other organs that most commonly affects children.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Henoch–Schönlein purpura · See more »

Hereditary elliptocytosis

Hereditary elliptocytosis, also known as ovalocytosis, is an inherited blood disorder in which an abnormally large number of the patient's erythrocytes (i.e. red blood cells) are elliptical rather than the typical biconcave disc shape.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hereditary elliptocytosis · See more »

Hereditary persistence of fetal hemoglobin

Hereditary persistence of fetal hemoglobin (HPFH, BrE: Hereditary persistence of foetal haemoglobin) is a benign condition in which significant fetal hemoglobin (hemoglobin F) production continues well into adulthood, disregarding the normal shutoff point after which only adult-type hemoglobin should be produced.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hereditary persistence of fetal hemoglobin · See more »

Hereditary spherocytosis

Hereditary spherocytosis (also known as Minkowski–Chauffard syndrome) is an abnormality of red blood cells, or erythrocytes.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hereditary spherocytosis · See more »

Hereditary stomatocytosis

Hereditary stomatocytosis describes a number of inherited autosomal dominant human conditions which affect the red blood cell, in which the membrane or outer coating of the cell 'leaks' sodium and potassium ions.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hereditary stomatocytosis · See more »

Heredity

Heredity is the passing on of traits from parents to their offspring, either through asexual reproduction or sexual reproduction, the offspring cells or organisms acquire the genetic information of their parents.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Heredity · See more »

Hexokinase deficiency

Hexokinase deficiency is an anemia-causing condition associated with inadequate hexokinase.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hexokinase deficiency · See more »

Histiocytosis

In medicine, histiocytosis is an excessive number of histiocytes (tissue macrophages), and the term is also often used to refer to a group of rare diseases which share this sign as a characteristic.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Histiocytosis · See more »

Humoral immune deficiency

Humoral immune deficiencies are conditions which cause impairment of humoral immunity, which can lead to immunodeficiency.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Humoral immune deficiency · See more »

Hyper IgM syndrome

Hyper IgM syndromes is a group of primary immune deficiency disorders characterized by defective CD40 signaling; via B cells affecting class switch recombination (CSR) and somatic hypermutation.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hyper IgM syndrome · See more »

Hypergammaglobulinemia

Hypergammaglobulinemia is a medical condition with elevated levels of gamma globulin.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hypergammaglobulinemia · See more »

Hyperimmunoglobulin E syndrome

Hyperimmunoglobulinemia E syndrome (HIES), of which the autosomal dominant form is called Job's syndrome or Buckley syndrome, is a heterogeneous group of immune disorders.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hyperimmunoglobulin E syndrome · See more »

Hypogammaglobulinemia

Hypogammaglobulinemia is a type of primary immunodeficiency disease in which not enough gamma globulins exist in the blood (thus hypo- + gamma + globulin + -emia).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hypogammaglobulinemia · See more »

Hypoplasia

Hypoplasia (from Ancient Greek ὑπo- hypo-, "under" + πλάσις plasis, "formation"; adjective form hypoplastic) is underdevelopment or incomplete development of a tissue or organ.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Hypoplasia · See more »

ICD-10

ICD-10 is the 10th revision of the International Statistical Classification of Diseases and Related Health Problems (ICD), a medical classification list by the World Health Organization (WHO).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and ICD-10 · See more »

ICD-10 Chapter I: Certain infectious and parasitic diseases

ICD-10 is an international statistical classification used in health care and related industries.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and ICD-10 Chapter I: Certain infectious and parasitic diseases · See more »

ICD-10 Chapter II: Neoplasms

ICD-10 is an international statistical classification used in health care and related industries.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and ICD-10 Chapter II: Neoplasms · See more »

IgG deficiency

IgG deficiency (Selective deficiency of immunoglobulin G) is a form of dysgammaglobulinemia where the proportional levels of the IgG isotype are reduced relative to other immunoglobulin isotypes.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and IgG deficiency · See more »

Immune system

The immune system is a host defense system comprising many biological structures and processes within an organism that protects against disease.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Immune system · See more »

Immune thrombocytopenic purpura

Immune thrombocytopenia (ITP) is a type of thrombocytopenic purpura defined as isolated low platelet count (thrombocytopenia) with normal bone marrow and the absence of other causes of thrombocytopenia.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Immune thrombocytopenic purpura · See more »

Immunodeficiency

Immunodeficiency (or immune deficiency) is a state in which the immune system's ability to fight infectious disease and cancer is compromised or entirely absent.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Immunodeficiency · See more »

Immunoglobulin A

Immunoglobulin A (IgA, also referred to as sIgA in its secretory form) is an antibody that plays a crucial role in the immune function of mucous membranes.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Immunoglobulin A · See more »

Immunoglobulin E

Immunoglobulin E (IgE) is a type of antibody (or immunoglobulin (Ig) "isotype") that has only been found in mammals.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Immunoglobulin E · See more »

Immunoglobulin G

Immunoglobulin G (IgG) is a type of antibody.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Immunoglobulin G · See more »

Immunoglobulin M

Immunoglobulin M (IgM) is one of several forms of antibody that are produced by vertebrates.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Immunoglobulin M · See more »

International Statistical Classification of Diseases and Related Health Problems

The International Classification of Diseases (ICD) is the international "standard diagnostic tool for epidemiology, health management and clinical purposes." Its full official name is International Statistical Classification of Diseases and Related Health Problems. The ICD is maintained by the World Health Organization (WHO), the directing and coordinating authority for health within the United Nations System.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and International Statistical Classification of Diseases and Related Health Problems · See more »

Intrinsic factor

Intrinsic factor (IF), also known as gastric intrinsic factor (GIF), is a glycoprotein produced by the parietal cells of the stomach.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Intrinsic factor · See more »

Iron deficiency

Iron deficiency, or sideropaenia, is the state in which a body has not enough (or not qualitatively enough) iron to supply its eventual needs.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Iron deficiency · See more »

Iron-deficiency anemia

Iron-deficiency anemia is anemia caused by a lack of iron.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Iron-deficiency anemia · See more »

Isolated primary immunoglobulin M deficiency

Isolated primary immunoglobulin M deficiency (or selective IgM immunodeficiency (SIgMD)) is a poorly defined dysgammaglobulinemia characterized by decreased levels of IgM while levels of other immunoglobulins are normal.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Isolated primary immunoglobulin M deficiency · See more »

Juvenile xanthogranuloma

Juvenile xanthogranuloma (JXG) is a form of histiocytosis, classified as "non-Langerhans cell histiocytosis", or more specifically, "type 2".

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Juvenile xanthogranuloma · See more »

Kostmann syndrome

Kostmann syndrome is a group of diseases that affect myelopoiesis, causing a congenital form of neutropenia (severe congenital neutropenia), usually without other physical malformations.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Kostmann syndrome · See more »

Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of Langerhans cells, abnormal cells deriving from bone marrow and capable of migrating from skin to lymph nodes.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Langerhans cell histiocytosis · See more »

Leukemia

Leukemia, also spelled leukaemia, is a group of cancers that usually begin in the bone marrow and result in high numbers of abnormal white blood cells.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Leukemia · See more »

Leukemoid reaction

The term leukemoid reaction describes an increased white blood cell count, or leukocytosis, which is a physiological response to stress or infection (as opposed to a primary blood malignancy, such as leukemia).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Leukemoid reaction · See more »

Leukocytosis

Leukocytosis is white cells (the leukocyte count) above the normal range in the blood.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Leukocytosis · See more »

List of ICD-9 codes 140–239: neoplasms

2.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and List of ICD-9 codes 140–239: neoplasms · See more »

Lung

The lungs are the primary organs of the respiratory system in humans and many other animals including a few fish and some snails.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Lung · See more »

Lymph node

A lymph node or lymph gland is an ovoid or kidney-shaped organ of the lymphatic system, and of the adaptive immune system, that is widely present throughout the body.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Lymph node · See more »

Lymphadenopathy

Lymphadenopathy or adenopathy is disease of the lymph nodes, in which they are abnormal in size, number, or consistency.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Lymphadenopathy · See more »

Lymphocyte function-associated antigen 1

Lymphocyte function-associated antigen 1 (LFA-1) is a cellular adhesion molecule found on lymphocytes.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Lymphocyte function-associated antigen 1 · See more »

Lymphocytopenia

Lymphocytopenia, or lymphopenia, is the condition of having an abnormally low level of lymphocytes in the blood.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Lymphocytopenia · See more »

Lymphocytosis

Lymphocytosis is an increase in the number of lymphocytes in the blood.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Lymphocytosis · See more »

Major histocompatibility complex

The major histocompatibility complex (MHC) is a set of cell surface proteins essential for the acquired immune system to recognize foreign molecules in vertebrates, which in turn determines histocompatibility.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Major histocompatibility complex · See more »

May–Hegglin anomaly

May–Hegglin anomaly (MHA), also known as Döhle leukocyte inclusions with giant platelets and macrothrombocytopenia with leukocyte inclusions, is a rare genetic disorder of the blood platelets that causes them to be abnormally large.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and May–Hegglin anomaly · See more »

Medical classification

Medical classification, or medical coding, is the process of transforming descriptions of medical diagnoses and procedures into universal medical code numbers.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Medical classification · See more »

Megaloblastic anemia

Megaloblastic anemia (or megaloblastic anaemia) is an anemia (of macrocytic classification) that results from inhibition of DNA synthesis during red blood cell production.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Megaloblastic anemia · See more »

Methemoglobinemia

Methemoglobinemia is a condition caused by elevated levels of methemoglobin in the blood.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Methemoglobinemia · See more »

MHC class I

MHC class I molecules are one of two primary classes of major histocompatibility complex (MHC) molecules (the other being MHC class II) and are found on the cell surface of all nucleated cells in the bodies of jawed vertebrates.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and MHC class I · See more »

Microangiopathic hemolytic anemia

In medicine (hematology), microangiopathic hemolytic anemia (MAHA) is a microangiopathic subgroup of hemolytic anemia (loss of red blood cells through destruction) caused by factors in the small blood vessels.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Microangiopathic hemolytic anemia · See more »

Monocytosis

Monocytosis is an increase in the number of monocytes circulating in the blood.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Monocytosis · See more »

Mononuclear phagocyte system

In immunology, the mononuclear phagocyte system or mononuclear phagocytic system (MPS) (also known as the reticuloendothelial system or macrophage system) is a part of the immune system that consists of the phagocytic cells located in reticular connective tissue.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Mononuclear phagocyte system · See more »

Multiple carboxylase deficiency

Multiple carboxylase deficiency is a form of metabolic disorder involving failures of carboxylation enzymes.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Multiple carboxylase deficiency · See more »

Myelophthisic anemia

Myelophthisic anemia (or myelophthisis) is a severe type of anemia found in some people with diseases that affect the bone marrow.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Myelophthisic anemia · See more »

Neutropenia

Neutropenia or neutropaenia is an abnormally low concentration of neutrophils (a type of white blood cell) in the blood.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Neutropenia · See more »

Neutrophil

Neutrophils (also known as neutrocytes) are the most abundant type of granulocytes and the most abundant (40% to 70%) type of white blood cells in most mammals.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Neutrophil · See more »

Nezelof syndrome

Nezelof syndrome (also known as Thymic dysplasia with normal immunoglobulins) is an autosomal recessive congenital immunodeficiency condition due to underdevelopment of the thymus.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Nezelof syndrome · See more »

Nonthrombocytopenic purpura

Nonthrombocytopenic purpura is a type of purpura (red or purple skin discoloration) not associated with thrombocytopenia.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Nonthrombocytopenic purpura · See more »

Nucleotide

Nucleotides are organic molecules that serve as the monomer units for forming the nucleic acid polymers deoxyribonucleic acid (DNA) and ribonucleic acid (RNA), both of which are essential biomolecules within all life-forms on Earth.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Nucleotide · See more »

Nutritional anemia

Nutritional anemia refers to the low concentration of hemoglobin due to poor diet.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Nutritional anemia · See more »

Paroxysmal cold hemoglobinuria

Paroxysmal cold hemoglobinuria (PCH), also known as Donath-Landsteiner syndrome, is a disease of humans that is characterized by the sudden presence of hemoglobin in the urine (called hemoglobinuria), typically after exposure to cold temperatures.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Paroxysmal cold hemoglobinuria · See more »

Paroxysmal nocturnal hemoglobinuria

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired, life-threatening disease of the blood characterized by destruction of red blood cells by the complement system, a part of the body's innate immune system.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Paroxysmal nocturnal hemoglobinuria · See more »

Pelger–Huet anomaly

Pelger–Huët anomaly (pronunciation) is a blood laminopathy associated with the lamin B receptor.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Pelger–Huet anomaly · See more »

Plasmacytosis

Plasmacytosis is a condition in which there is an unusually large proportion of plasma cells in tissues, exudates, or blood.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Plasmacytosis · See more »

Platelet

Platelets, also called thrombocytes (from Greek θρόμβος, "clot" and κύτος, "cell"), are a component of blood whose function (along with the coagulation factors) is to react to bleeding from blood vessel injury by clumping, thereby initiating a blood clot.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Platelet · See more »

Plummer–Vinson syndrome

Plummer–Vinson syndrome (PVS), also called Paterson–Brown–Kelly syndrome or sideropenic dysphagia, is a rare disease characterized by difficulty in swallowing, iron-deficiency anemia, glossitis, cheilosis and esophageal webs.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Plummer–Vinson syndrome · See more »

Polyclonal antibodies

Polyclonal antibodies (pAbs) are antibodies that are secreted by different B cell lineages within the body (whereas monoclonal antibodies come from a single cell lineage).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Polyclonal antibodies · See more »

Polycythemia

Polycythemia (also known as polycythaemia or polyglobulia) is a disease state in which the hematocrit (the volume percentage of red blood cells in the blood) is elevated.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Polycythemia · See more »

Proteinuria

Proteinuria is the presence of excess proteins in the urine.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Proteinuria · See more »

Pure red cell aplasia

Pure red cell aplasia (PRCA) or erythroblastopenia refers to a type of anemia affecting the precursors to red blood cells but not to white blood cells.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Pure red cell aplasia · See more »

Purine nucleoside phosphorylase deficiency

Purine nucleoside phosphorylase deficiency, often called PNP-deficiency, is a rare autosomal recessive metabolic disorder which results in immunodeficiency.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Purine nucleoside phosphorylase deficiency · See more »

Purpura

Purpura is a condition of red or purple discolored spots on the skin that do not blanch on applying pressure.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Purpura · See more »

Purpura fulminans

Purpura fulminans is an acute, often fatal, thrombotic disorder which manifests as blood spots, bruising and discolouration of the skin resulting from coagulation in small blood vessels within the skin and rapidly leads to skin necrosis and disseminated intravascular coagulation.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Purpura fulminans · See more »

Pyruvate kinase deficiency

Pyruvate kinase deficiency is an inherited metabolic disorder of the enzyme pyruvate kinase which affects the survival of red blood cells.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Pyruvate kinase deficiency · See more »

Qualitative property

Qualitative properties are properties that are observed and can generally not be measured with a numerical result.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Qualitative property · See more »

Reticular dysgenesis

Reticular dysgenesis (RD) is a rare, inherited autosomal recessive disease that results in immunodeficiency.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Reticular dysgenesis · See more »

Reticulohistiocytoma

Reticulohistiocytoma is a cutaneous condition characterized by a solitary, firm, dermal skin lesion of less than 1 cm in diameter.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Reticulohistiocytoma · See more »

Rosai–Dorfman disease

Rosai–Dorfman disease, originally known as sinus histiocytosis with massive lymphadenopathy, is a rare disorder of unknown cause that is characterized by abundant histiocytes in the lymph nodes or other locations throughout the body.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Rosai–Dorfman disease · See more »

Sarcoidosis

Sarcoidosis is a disease involving abnormal collections of inflammatory cells that form lumps known as granulomas.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Sarcoidosis · See more »

Scurvy

Scurvy is a disease resulting from a lack of vitamin C (ascorbic acid).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Scurvy · See more »

Selective immunoglobulin A deficiency

Selective immunoglobulin A (IgA) deficiency (SIgAD) is a genetic immunodeficiency, a type of hypogammaglobulinemia.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Selective immunoglobulin A deficiency · See more »

Sepsis

Sepsis is a life-threatening condition that arises when the body's response to infection causes injury to its own tissues and organs.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Sepsis · See more »

Severe combined immunodeficiency

Severe combined immunodeficiency, SCID, also known as alymphocytosis, Glanzmann–Riniker syndrome, severe mixed immunodeficiency syndrome, and thymic alymphoplasia, is a rare genetic disorder characterized by the disturbed development of functional T cells and B cells caused by numerous genetic mutations that result in heterogeneous clinical presentations.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Severe combined immunodeficiency · See more »

Sickle cell disease

Sickle cell disease (SCD) is a group of blood disorders typically inherited from a person's parents.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Sickle cell disease · See more »

Sickle cell trait

Sickle cell trait describes a condition in which a person has one abnormal allele of the hemoglobin beta gene (is heterozygous), but does not display the severe symptoms of sickle-cell disease that occur in a person who has two copies of that allele (is homozygous).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Sickle cell trait · See more »

Sideroblastic anemia

Sideroblastic anemia or sideroachrestic anemia is a form of anemia in which the bone marrow produces ringed sideroblasts rather than healthy red blood cells (erythrocytes).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Sideroblastic anemia · See more »

Skin

Skin is the soft outer tissue covering vertebrates.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Skin · See more »

Southeast Asian ovalocytosis

Southeast Asian ovalocytosis is a blood disorder that is similar to, but distinct from hereditary elliptocytosis.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Southeast Asian ovalocytosis · See more »

Spleen

The spleen is an organ found in virtually all vertebrates.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Spleen · See more »

Splenic infarction

Splenic infarction is a condition in which oxygen supply to the spleen is interrupted, leading to partial or complete infarction (tissue death due to oxygen shortage) in the organ.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Splenic infarction · See more »

Splenomegaly

Splenomegaly is an enlargement of the spleen.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Splenomegaly · See more »

Sulfhemoglobinemia

Sulfhemoglobinemia (or sulfhaemoglobinaemia) is a rare condition in which there is excess sulfhemoglobin (SulfHb) in the blood.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Sulfhemoglobinemia · See more »

T cell

A T cell, or T lymphocyte, is a type of lymphocyte (a subtype of white blood cell) that plays a central role in cell-mediated immunity.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and T cell · See more »

Thalassemia

Thalassemias are inherited blood disorders characterized by abnormal hemoglobin production.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Thalassemia · See more »

Thrombocytopenia

Thrombocytopenia is a condition characterized by abnormally low levels of thrombocytes, also known as platelets, in the blood.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Thrombocytopenia · See more »

Transcobalamin

Transcobalamins are carrier proteins which bind cobalamin (B12).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Transcobalamin · See more »

Transient hypogammaglobulinemia of infancy

Transient hypogammaglobulinemia of infancy is a form of hypogammaglobulinemia appearing after birth, leading to a reduction in the level of IgG, and also sometimes IgA and IgM.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Transient hypogammaglobulinemia of infancy · See more »

Triosephosphate isomerase deficiency

Triosephosphate isomerase deficiency is a rare autosomal recessive metabolic disorder which was initially described in 1965.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Triosephosphate isomerase deficiency · See more »

Vitamin B12

Vitamin B12, also called cobalamin, is a water-soluble vitamin that is involved in the metabolism of every cell of the human body: it is a cofactor in DNA synthesis, and in both fatty acid and amino acid metabolism.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Vitamin B12 · See more »

Vitamin B12 deficiency anemia

Vitamin B12 deficiency anemia, of which pernicious anemia is a type, is a disease in which not enough red blood cells are produced due to a deficiency of vitamin B12.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Vitamin B12 deficiency anemia · See more »

Von Willebrand disease

Von Willebrand disease (vWD) is the most common hereditary blood-clotting disorder in humans.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Von Willebrand disease · See more »

Warm antibody autoimmune hemolytic anemia

Warm antibody autoimmune hemolytic anemia (WAIHA) is the most common form of autoimmune hemolytic anemia.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Warm antibody autoimmune hemolytic anemia · See more »

White blood cell

White blood cells (WBCs), also called leukocytes or leucocytes, are the cells of the immune system that are involved in protecting the body against both infectious disease and foreign invaders.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and White blood cell · See more »

Wiskott–Aldrich syndrome

Wiskott–Aldrich syndrome (WAS) is a rare X-linked recessive disease characterized by eczema, thrombocytopenia (low platelet count), immune deficiency, and bloody diarrhea (secondary to the thrombocytopenia).

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and Wiskott–Aldrich syndrome · See more »

World Health Organization

The World Health Organization (WHO; French: Organisation mondiale de la santé) is a specialized agency of the United Nations that is concerned with international public health.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and World Health Organization · See more »

X-linked agammaglobulinemia

X-linked agammaglobulinemia (XLA) is a rare genetic disorder discovered in 1952 that affects the body's ability to fight infection.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and X-linked agammaglobulinemia · See more »

X-linked lymphoproliferative disease

X-linked lymphoproliferative disease (also known as "Duncan's disease" or "Purtilo syndrome") is a lymphoproliferative disorder.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and X-linked lymphoproliferative disease · See more »

X-linked severe combined immunodeficiency

X-linked severe combined immunodeficiency (X-SCID) is an immunodeficiency disorder in which the body produces very few T cells and NK cells.

New!!: ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism and X-linked severe combined immunodeficiency · See more »

Redirects here:

ICD-10 Chapter D, ICD-10 Chapter II: Neoplasms; Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism, ICD-10 Chapters C and D: Neoplasms, diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism.

References

[1] https://en.wikipedia.org/wiki/ICD-10_Chapter_III:_Diseases_of_the_blood_and_blood-forming_organs,_and_certain_disorders_involving_the_immune_mechanism

OutgoingIncoming
Hey! We are on Facebook now! »