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115 relations: Acalypha indica, Anemia, Aspirin, Asymptomatic, Autoimmune hemolytic anemia, Barton Childs, Beutler test, Centre for Arab Genomic Studies, Chilean recluse spider, Chlorproguanil/dapsone, Chlorproguanil/dapsone/artesunate, Chronic granulomatous disease, Congenital hemolytic anemia, Dapsone, Degmacyte, Dengue fever, Divicine, Drug-induced nonautoimmune hemolytic anemia, Dunbar High School (Washington, D.C.), Elimination diet, Food and drink prohibitions, Food intolerance, Genetic studies on Arabs, Gilbert's syndrome, Glucose 6-phosphate, Glucose-6-phosphate dehydrogenase, Glutathione reductase, Glycated hemoglobin, Habibollah Hedayat, Hematologic disease, Hemoglobinopathy, Hemoglobinuria, Hemolysis, Hemolytic anemia, Henna, Hepatitis E, History of malaria, HK1, Human genetic resistance to malaria, ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism, Inborn errors of carbohydrate metabolism, Inborn errors of metabolism, Isobutyl nitrite, Isoniazid/pyridoxine/sulfamethoxazole/trimethoprim, James E. Bowman, Jaundice, Kernicterus, L-gulonolactone oxidase, Lethal allele, Lidia Mannuzzu, ..., List of causes of hypoglycemia, List of diseases (G), List of diseases (H), List of disorders included in newborn screening programs, List of genetic disorders, List of hematologic conditions, List of MeSH codes (C15), List of MeSH codes (C16), List of MeSH codes (C18), List of MeSH codes (C21), Macrocytic anemia, Malaria, Marcello Siniscalco, Mass drug administration, Medical genetics of Jews, Melarsoprol, Menadione, Methemoglobin, Methemoglobinemia, Methylene blue, Mothball, Naphthalene, Neonatal jaundice, Neonatal red cell transfusion, Nitrofurantoin, Nitrofurazone, Nitrogen dioxide poisoning, Oliguria, Pamaquine, Parsi, Pea, Pegloticase, Pentose phosphate pathway, Pharmacogenomics, Phenacetin, Phenazopyridine, Plasmodium falciparum, Priapism, Primaquine, Propyphenazone/paracetamol/caffeine, Prussian blue (medical use), Pyknocytosis, Pyruvate kinase deficiency, Quinine, Rasburicase, Red blood cell, Rhabdomyolysis, Ribose-phosphate diphosphokinase, Rickettsia rickettsii, Sephardi Jews, Sex linkage, Sickle cell disease, Sulfasalazine, Sweat test, Tafenoquine, Transaldolase deficiency, Vatalia, Vicia, Vicia faba, Vicine, X-linked recessive inheritance, 1000 Genomes Project, 4-Aminosalicylic acid, 6-phosphogluconate dehydrogenase deficiency, 8-Aminoquinoline. Expand index (65 more) »
Acalypha indica
Acalypha indica (English: Indian Acalypha, Indian Mercury, Indian Copperleaf, Indian Nettle, Three-seeded Mercury) is an herbaceous annual that has catkin-like inflorescences with cup-shaped involucres surrounding the minute flowers.
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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.
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Aspirin
Aspirin, also known as acetylsalicylic acid (ASA), is a medication used to treat pain, fever, or inflammation.
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Asymptomatic
In medicine, a disease is considered asymptomatic if a patient is a carrier for a disease or infection but experiences no symptoms.
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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.
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Barton Childs
Barton Childs (February 29, 1916 – February 18, 2010) was an American pediatrician and geneticist.
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Beutler test
The Beutler test, also known as the fluorescent spot test, is a screening test used to identify enzyme defects.
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Centre for Arab Genomic Studies
The Centre for Arab Genomic Studies (CAGS) is a not-for-profit study centre aimed at the characterization and prevention of genetic disorders in the Arab World.
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Chilean recluse spider
The Chilean recluse spider is a venomous spider, Loxosceles laeta, of the family Sicariidae (formerly of the family Loxoscelidae).
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Chlorproguanil/dapsone
Chlorproguanil/dapsone (sold commercially as Lapdap) was a fixed dose antimalarial combination containing chlorproguanil and dapsone, which act synergystically against malaria.
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Chlorproguanil/dapsone/artesunate
Chlorproguanil/dapsone/artesunate (abbreviated CDA) was an experimental antimalarial treatment that entered Phase III clinical trials in 2006.
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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.
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Congenital hemolytic anemia
Congenital hemolytic anemia (or hereditary hemolytic anemia) refers to hemolytic anemia which is primarily due to congenital disorders.
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Dapsone
Dapsone, also known as diaminodiphenyl sulfone (DDS), is an antibiotic commonly used in combination with rifampicin and clofazimine for the treatment of leprosy.
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Degmacyte
A degmacyte (a.k.a. "bite cell") is an abnormally shaped red blood cell with one or more semicircular portions removed from the cell margin.
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Dengue fever
Dengue fever is a mosquito-borne tropical disease caused by the dengue virus.
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Divicine
Divicine (2,6-diamino-4,5-dihydroxypyrimidine) is an oxidant and a base with alkaloidal properties found in fava beans and Lathyrus sativus.
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Drug-induced nonautoimmune hemolytic anemia
Drug-induced nonautoimmune hemolytic anemia is a form of hemolytic anemia.
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Dunbar High School (Washington, D.C.)
Paul Laurence Dunbar High School is a public secondary school located in Washington, D.C., United States. The school is located in the Truxton Circle neighborhood of Northwest Washington, two blocks from the intersection of New Jersey and New York avenues. Dunbar, which serves grades 9 through 12, is a part of the District of Columbia Public Schools. From the early 20th century to the 1950s, Dunbar became known as the classical academic high school for black students in the segregated public schools. As all public school teachers were federal civil servants, its teachers received pay equal to that of white teachers in other schools in the district. It attracted high-quality faculty, many with advanced degrees, including doctorates. Parents sent their children to the high school from across the city because of its high standards. Many of its alumni graduated from top-quality colleges and universities, and gained professional degrees.
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Elimination diet
An elimination diet, also known as exclusion diet is a diagnostic procedure used to identify foods that an individual cannot consume without adverse effects.
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Food and drink prohibitions
Some people abstain from consuming various foods and beverages in conformity with various religious, cultural, legal or other societal prohibitions.
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Food intolerance
Food intolerance is a detrimental reaction, often delayed, to a food, beverage, food additive, or compound found in foods that produces symptoms in one or more body organs and systems, but generally refers to reactions other than food allergy.
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Genetic studies on Arabs
The Centre for Arab Genomic Studies (CAGS) oversees genetic analyses on the populations of the Arab world.
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Gilbert's syndrome
Gilbert's syndrome (GS) is a mild liver disorder in which the liver does not properly process bilirubin.
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Glucose 6-phosphate
Glucose 6-phosphate (sometimes called the Robison ester) is a glucose sugar phosphorylated at the hydroxy group on carbon 6.
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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).
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Glutathione reductase
Glutathione reductase (GR) also known as glutathione-disulfide reductase (GSR) is an enzyme that in humans is encoded by the GSR gene.
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Glycated hemoglobin
Glycated hemoglobin (hemoglobin A1c, HbA1c, A1C, or Hb1c; sometimes also referred to as being Hb1c or HGBA1C) is a form of hemoglobin that is measured primarily to identify the three-month average plasma glucose concentration.
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Habibollah Hedayat
Dr.
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Hematologic disease
Hematologic diseases are disorders which primarily affect the blood.
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Hemoglobinopathy
Hemoglobinopathy is a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule.
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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.
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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).
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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).
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Henna
Henna (حِنَّاء) is a dye prepared from the plant Lawsonia inermis, also known as hina, the henna tree, the mignonette tree, and the Egyptian privet, the sole species of the genus Lawsonia.
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Hepatitis E
Hepatitis E is a viral hepatitis (liver inflammation) caused by infection with a virus called hepatitis E virus.
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History of malaria
The history of malaria stretches from its prehistoric origin as a zoonotic disease in the primates of Africa through to the 21st century.
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HK1
Hexokinase-1 (HK1) is an enzyme that in humans is encoded by the HK1 gene on chromosome 10.
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Human genetic resistance to malaria
Human genetic resistance to malaria refers to inherited changes in the DNA of humans which increase resistance to malaria and result in increased survival of individuals with those genetic changes.
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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.
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Inborn errors of carbohydrate metabolism
Inborn errors of carbohydrate metabolism are inborn error of metabolism that affect the catabolism and anabolism of carbohydrates.
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Inborn errors of metabolism
Inborn errors of metabolism form a large class of genetic diseases involving congenital disorders of metabolism.
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Isobutyl nitrite
Isobutyl nitrite, C4H9NO2, is an alkyl nitrite, an ester of isobutanol and nitrous acid.
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Isoniazid/pyridoxine/sulfamethoxazole/trimethoprim
Isoniazid/pyridoxine/sulfamethoxazole/trimethoprim (INH/B6/CTX) is a fixed dose combination medication for the prevention of opportunistic infections in HIV/AIDS.
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James E. Bowman
James Edward Bowman Jr. (February 5, 1923 – September 28, 2011) was an American physician and specialist in pathology, hematology, and genetics.
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Jaundice
Jaundice, also known as icterus, is a yellowish or greenish pigmentation of the skin and whites of the eyes due to high bilirubin levels.
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Kernicterus
Kernicterus is a bilirubin-induced brain dysfunction.
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L-gulonolactone oxidase
L-gulonolactone oxidase (EC) is an enzyme that produces vitamin C, but is non-functional in Haplorrhini (including humans), in some bats, and in guinea pigs.
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Lethal allele
Lethal alleles (also referred to as lethal genes or lethals) are alleles that cause the death of the organism that carries them.
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Lidia Mannuzzu
Lidia Mannuzzu (21 April 1958 – 24 October 2016) was an Italian biologist, physiologist and academic.
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List of causes of hypoglycemia
Hypoglycemia is a common problem in critically ill or extremely low birthweight infants.
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List of diseases (G)
This is a list of diseases starting with the letter "G".
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List of diseases (H)
This is a list of diseases starting with the letter "H".
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List of disorders included in newborn screening programs
This is a list of disorders included in newborn screening programs around the world, along with information on testing methodologies, disease incidence and rationale for being included in screening programs.
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List of genetic disorders
The following is a list of genetic disorders and if known, type of mutation and the chromosome involved.
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List of hematologic conditions
There are many conditions of or affecting the human hematologic system — the biological system that includes plasma, platelets, leukocytes, and erythrocytes, the major components of blood and the bone marrow.
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List of MeSH codes (C15)
The following is a list of the "C" codes for MeSH.
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List of MeSH codes (C16)
The following is a list of the "C" codes for MeSH.
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List of MeSH codes (C18)
The following is a list of the "C" codes for MeSH.
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List of MeSH codes (C21)
The following is a list of the "C" codes for MeSH.
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Macrocytic anemia
The term macrocytic is from Greek words meaning "large cell".
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Malaria
Malaria is a mosquito-borne infectious disease affecting humans and other animals caused by parasitic protozoans (a group of single-celled microorganisms) belonging to the Plasmodium type.
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Marcello Siniscalco
Marcello Siniscalco (31 July 1924 – 29 November 2013) was an Italian scientist at the forefront of the development of the nascent field of genetics.
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Mass drug administration
The administration of drugs to whole populations irrespective of disease status is referred to as mass drug administration (MDA).
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Medical genetics of Jews
The medical genetics of Jews is the study, screening, and treatment of genetic disorders more common in particular Jewish populations than in the population as a whole.
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Melarsoprol
Melarsoprol is a medication used for the treatment of sleeping sickness (African trypanosomiasis).
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Menadione
Menadione is an organic compound with the formula C6H4(CO)2C2H(CH3).
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Methemoglobin
Methemoglobin (English: methaemoglobin) (pronounced "met-hemoglobin") is a form of the oxygen-carrying metalloprotein hemoglobin, in which the iron in the heme group is in the Fe3+ (ferric) state, not the Fe2+ (ferrous) of normal hemoglobin.
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Methemoglobinemia
Methemoglobinemia is a condition caused by elevated levels of methemoglobin in the blood.
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Methylene blue
Methylene blue, also known as methylthioninium chloride, is a medication and dye.
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Mothball
Mothballs are small balls of chemical pesticide and deodorant, sometimes used when storing clothing and other articles susceptible to damage from mold or moth larvae (especially clothes moths like Tineola bisselliella).
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Naphthalene
Naphthalene is an organic compound with formula.
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Neonatal jaundice
Neonatal jaundice is a yellowish discoloration of the white part of the eyes and skin in a newborn baby due to high bilirubin levels.
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Neonatal red cell transfusion
Neonates are defined as babies up to 28 days after birth.
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Nitrofurantoin
Nitrofurantoin, sold under the trade name Macrobid among others, is an antibiotic used to treat bladder infections.
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Nitrofurazone
Nitrofurazone (INN, trade name Furacin) is an antimicrobial organic compound belonging to the furan class.
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Nitrogen dioxide poisoning
Nitrogen dioxide poisoning is the illness resulting from the toxic effect of nitrogen dioxide.
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Oliguria
Oliguria or hypouresis (both names from roots meaning "not enough urine") is the low output of urine.
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Pamaquine
Pamaquine is an 8-aminoquinoline drug used for the treatment of malaria.
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Parsi
A Parsi (or Parsee) means "Persian" in the "Persian Language", which today mainly refers to a member of a Zoroastrian community, one of two (the other being Iranis) mainly located in India, with a few in Pakistan.
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Pea
The pea is most commonly the small spherical seed or the seed-pod of the pod fruit Pisum sativum.
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Pegloticase
Pegloticase (trade name Krystexxa) is a medication for the treatment of severe, treatment-refractory, chronic gout.
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Pentose phosphate pathway
The pentose phosphate pathway (also called the phosphogluconate pathway and the hexose monophosphate shunt) is a metabolic pathway parallel to glycolysis.
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Pharmacogenomics
Pharmacogenomics is the study of the role of the genome in drug response.
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Phenacetin
Phenacetin (or acetophenetidin) is a pain-relieving and fever-reducing drug, which was widely used between its introduction in 1887 and the 1983 ban imposed by the U.S. Food and Drug Administration.
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Phenazopyridine
Phenazopyridine is a chemical which, when excreted into the urine, has a local analgesic effect.
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Plasmodium falciparum
Plasmodium falciparum is a unicellular protozoan parasite of humans, and the deadliest species of Plasmodium that cause malaria in humans.
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Priapism
Priapism is a condition in which a penis remains erect for hours in the absence of stimulation or after stimulation has ended.
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Primaquine
Primaquine is a medication used to treat and prevent malaria and to treat ''Pneumocystis'' pneumonia.
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Propyphenazone/paracetamol/caffeine
Propyphenazone/paracetamol/caffeine (trade name Saridon) is an analgesic combination indicated for the management of headache.
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Prussian blue (medical use)
Prussian blue, also known as potassium ferric hexacyanoferrate, is used as a medication to treat thallium poisoning or radioactive cesium poisoning.
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Pyknocytosis
Pyknocytosis is a hematologic state characterized by the presence of pyknocytes in the blood.
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Pyruvate kinase deficiency
Pyruvate kinase deficiency is an inherited metabolic disorder of the enzyme pyruvate kinase which affects the survival of red blood cells.
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Quinine
Quinine is a medication used to treat malaria and babesiosis.
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Rasburicase
Rasburicase (trade names Elitek in the US and Fasturtec in Europe) is a medication that helps to clear uric acid from the blood.
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Red blood cell
Red blood cells-- also known as RBCs, red cells, red blood corpuscles, haematids, erythroid cells or erythrocytes (from Greek erythros for "red" and kytos for "hollow vessel", with -cyte translated as "cell" in modern usage), are the most common type of blood cell and the vertebrate's principal means of delivering oxygen (O2) to the body tissues—via blood flow through the circulatory system.
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Rhabdomyolysis
Rhabdomyolysis is a condition in which damaged skeletal muscle breaks down rapidly.
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Ribose-phosphate diphosphokinase
Ribose-phosphate diphosphokinase (or phosphoribosyl pyrophosphate synthetase or ribose-phosphate pyrophosphokinase) is an enzyme that converts ribose 5-phosphate into phosphoribosyl pyrophosphate (PRPP).
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Rickettsia rickettsii
Rickettsia rickettsii (abbreviated as R. rickettsii) is a gram-negative, intracellular, coccobacillus bacterium that is around 0.8 to 2.0 micrometers long.
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Sephardi Jews
Sephardi Jews, also known as Sephardic Jews or Sephardim (סְפָרַדִּים, Modern Hebrew: Sefaraddim, Tiberian: Səp̄āraddîm; also Ye'hude Sepharad, lit. "The Jews of Spain"), originally from Sepharad, Spain or the Iberian peninsula, are a Jewish ethnic division.
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Sex linkage
Sex linkage is the phenotypic expression of an allele related to the allosome (sex chromosome) of the individual.
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Sickle cell disease
Sickle cell disease (SCD) is a group of blood disorders typically inherited from a person's parents.
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Sulfasalazine
Sulfasalazine (SSZ), sold under the trade name Azulfidine among others, is a medication used to treat rheumatoid arthritis, ulcerative colitis, and Crohn's disease.
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Sweat test
The sweat test measures the concentration of chloride that is excreted in sweat.
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Tafenoquine
Tafenoquine is an 8-aminoquinoline drug manufactured by GlaxoSmithKline that is being investigated as a potential treatment for malaria, as well as for malaria prevention.
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Transaldolase deficiency
Transaldolase deficiency is a disease characterised by abnormally low levels of the Transaldolase enzyme.
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Vatalia
Vatalia or Vataliya Prajapati are an endogamous Hindu group and a sub-caste of Prajapati or Kumbhar caste found only in Gujarat and are among the Socially and Educationally Backward Classes of Gujarat, India.
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Vicia
Vicia is a genus of about 140 species of flowering plants that are part of the legume family (Fabaceae), and which are commonly known as vetches.
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Vicia faba
Vicia faba, also known as the broad bean, fava bean, faba bean, field bean, bell bean, or tic bean, is a species of flowering plant in the pea and bean family Fabaceae.
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Vicine
Vicine is an alkaloid glycoside found in fava beans.
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X-linked recessive inheritance
X-linked recessive inheritance is a mode of inheritance in which a mutation in a gene on the X chromosome causes the phenotype to be expressed in males (who are necessarily hemizygous for the gene mutation because they have one X and one Y chromosome) and in females who are homozygous for the gene mutation, see zygosity.
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1000 Genomes Project
The 1000 Genomes Project (abbreviated as 1KGP), launched in January 2008, was an international research effort to establish by far the most detailed catalogue of human genetic variation.
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4-Aminosalicylic acid
4-Aminosalicylic acid, also known as para-aminosalicylic acid (PAS) is an antibiotic primarily used to treat tuberculosis.
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6-phosphogluconate dehydrogenase deficiency
6-Phosphogluconate dehydrogenase deficiency (6PGD deficiency), or partial deficiency, is an autosomal hereditary disease characterized by abnormally low levels of 6-Phosphogluconate dehydrogenase (6PGD), a metabolic enzyme involved in the Pentose phosphate pathway.
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8-Aminoquinoline
8-Aminoquinoline is a form of aminoquinoline with an amine at the 8-position of quinoline.
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Favism, G6PD Deficiency, G6PD defficiency, G6PD deficiency, G6PD deficiency anaemia, G6PDD, G6PDH deficiency, G6pd deficiency, G6pdd, Glucose 6 phosphate dehydrogenase deficiency, Glucose 6-phosphate dehydrogenase deficiency, Glucose-6-Phosphatase Dehydrogenase deficiency, Glucose-6-Phosphate Dehydrogenase deficiency, Glucose-6-dehydrogenase deficiency, Glucosephosphate dehydrogenase deficiency, Hereditary non-spherocytic hemolytic anemia.
References
[1] https://en.wikipedia.org/wiki/Glucose-6-phosphate_dehydrogenase_deficiency
