+ acanthocytosis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14071758-n
|
the presence of acanthocytes in the blood stream (as in abetalipoproteinemia)
|
+ acidemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14020753-n
|
a blood disorder characterized by an increased concentration of hydrogen ions in the blood (which falls below 7 on the pH scale)
|
+ afibrinogenemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14170623-n
|
the absence of fibrinogen in the plasma leading to prolonged bleeding
|
+ agranulocytic
|
a
|
1
|
[ blood_disease ]
|
eng-30-02608380-a
|
relating to the blood disorder of agranulocytosis
|
+ agranulocytosis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14071896-n
|
an acute blood disorder (often caused by radiation or drug therapy) characterized by severe reduction in granulocytes
|
+ agranulosis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14071896-n
|
an acute blood disorder (often caused by radiation or drug therapy) characterized by severe reduction in granulocytes
|
+ alkalemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14020936-n
|
a blood disorder characterized by a lower concentration of hydrogen ions in the blood (which rises above 7.45 on the pH scale)
|
+ anaemia
|
n
|
2
|
[ blood_disease ]
|
eng-30-14195315-n
|
a deficiency of red blood cells
|
+ anaemic
|
a
|
1
|
[ blood_disease ]
|
eng-30-03041331-a
|
relating to anemia or suffering from anemia
|
+ analbuminemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14072126-n
|
an abnormally low level of albumin in the blood serum
|
+ anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14195315-n
|
a deficiency of red blood cells
|
+ anemic
|
a
|
2
|
[ blood_disease ]
|
eng-30-03041331-a
|
relating to anemia or suffering from anemia
|
+ angiohemophilia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14171176-n
|
a form of hemophilia discovered by Erik von Willebrand; a genetic disorder that is inherited as an autosomal recessive trait; characterized by a deficiency of the coagulation factor and by mucosal bleeding
|
+ aplastic_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14164341-n
|
anemia characterized by pancytopenia resulting from failure of the bone marrow; can be caused by neoplasm or by toxic exposure
|
+ aplastic_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14164341-n
|
anemia characterized by pancytopenia resulting from failure of the bone marrow; can be caused by neoplasm or by toxic exposure
|
+ Banti's_disease
|
n
|
1
|
[ blood_disease ]
|
eng-30-14072239-n
|
a disease characterized by congestion and enlargement of the spleen; accompanied by anemia or cirrhosis
|
+ Banti's_syndrome
|
n
|
1
|
[ blood_disease ]
|
eng-30-14072239-n
|
a disease characterized by congestion and enlargement of the spleen; accompanied by anemia or cirrhosis
|
+ bleeder's_disease
|
n
|
1
|
[ blood_disease ]
|
eng-30-14170337-n
|
congenital tendency to uncontrolled bleeding; usually affects males and is transmitted from mother to son
|
+ blood_poisoning
|
n
|
1
|
[ blood_disease ]
|
eng-30-14189837-n
|
invasion of the bloodstream by virulent microorganisms from a focus of infection
|
+ childbed_fever
|
n
|
1
|
[ blood_disease ]
|
eng-30-14190493-n
|
serious form of septicemia contracted by a woman during childbirth or abortion (usually attributable to unsanitary conditions); formerly widespread but now uncommon
|
+ chlorosis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14166775-n
|
iron deficiency anemia in young women; characterized by weakness and menstrual disturbances and a green color to the skin
|
+ chlorotic
|
a
|
1
|
[ blood_disease ]
|
eng-30-02695389-a
|
of or pertaining to or suffering from chlorosis
|
+ Christmas_disease
|
n
|
1
|
[ blood_disease ]
|
eng-30-14170987-n
|
a clotting disorder similar to hemophilia A but caused by a congenital deficiency of factor IX
|
+ classical_haemophilia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14170772-n
|
hemophilia caused by a congenital deficiency of factor VIII; occurs almost exclusively in men
|
+ classical_hemophilia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14170772-n
|
hemophilia caused by a congenital deficiency of factor VIII; occurs almost exclusively in men
|
+ crescent-cell_anaemia
|
n
|
1
|
[ congenital_disease blood_disease ]
|
eng-30-14168792-n
|
a congenital form of anemia occurring mostly in blacks; characterized by abnormal blood cells having a crescent shape
|
+ crescent-cell_anemia
|
n
|
1
|
[ congenital_disease blood_disease ]
|
eng-30-14168792-n
|
a congenital form of anemia occurring mostly in blacks; characterized by abnormal blood cells having a crescent shape
|
+ cyclic_neutropenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14196722-n
|
neutropenia that occurs periodically
|
+ cytopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-13973490-n
|
a deficiency of some cellular element of the blood
|
+ drepanocytic_anaemia
|
n
|
1
|
[ congenital_disease blood_disease ]
|
eng-30-14168792-n
|
a congenital form of anemia occurring mostly in blacks; characterized by abnormal blood cells having a crescent shape
|
+ drepanocytic_anemia
|
n
|
1
|
[ congenital_disease blood_disease ]
|
eng-30-14168792-n
|
a congenital form of anemia occurring mostly in blacks; characterized by abnormal blood cells having a crescent shape
|
+ erythroblastosis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14191756-n
|
a blood disease characterized by the abnormal presence of erythroblasts in the blood
|
+ erythroblastosis_fetalis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14164548-n
|
severe anemia in newborn babies; the result of Rh incompatibility between maternal and fetal blood; typically occurs when the child of an Rh-negative mother inherits Rh-positive blood from the father; can be diagnosed before birth by amniocentesis
|
+ essential_thrombocytopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14197780-n
|
the primary form of thrombocytopenia (rather than a shortage of platelets caused by other conditions such as tuberculosis or chemical suppression of bone marrow etc.)
|
+ favism
|
n
|
1
|
[ blood_disease ]
|
eng-30-14165081-n
|
anemia resulting from eating fava beans; victims have an inherited blood abnormality and enzyme deficiency
|
+ fowl_cholera
|
n
|
1
|
[ disease blood_disease ]
|
eng-30-14263562-n
|
an acute diarrheal disease (especially of chickens) caused by the microorganism that causes hemorrhagic septicemia
|
+ granulocytopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14071896-n
|
an acute blood disorder (often caused by radiation or drug therapy) characterized by severe reduction in granulocytes
|
+ greensick
|
a
|
1
|
[ blood_disease ]
|
eng-30-02695389-a
|
of or pertaining to or suffering from chlorosis
|
+ greensickness
|
n
|
1
|
[ blood_disease ]
|
eng-30-14166775-n
|
iron deficiency anemia in young women; characterized by weakness and menstrual disturbances and a green color to the skin
|
+ haematocytopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-13973632-n
|
an abnormally low number of red blood cells in the blood
|
+ haemoglobinopathy
|
n
|
1
|
[ blood_disease ]
|
eng-30-14192034-n
|
a blood disease characterized by the presence of abnormal hemoglobins in the blood
|
+ haemolytic_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14165240-n
|
anemia resulting from destruction of erythrocytes
|
+ haemophilia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14170337-n
|
congenital tendency to uncontrolled bleeding; usually affects males and is transmitted from mother to son
|
+ haemophilia_A
|
n
|
1
|
[ blood_disease ]
|
eng-30-14170772-n
|
hemophilia caused by a congenital deficiency of factor VIII; occurs almost exclusively in men
|
+ haemophilia_B
|
n
|
1
|
[ blood_disease ]
|
eng-30-14170987-n
|
a clotting disorder similar to hemophilia A but caused by a congenital deficiency of factor IX
|
+ haemophilic
|
a
|
1
|
[ blood_disease ]
|
eng-30-02850826-a
|
relating to or having hemophilia
|
+ Hand-Schuller-Christian_disease
|
n
|
1
|
[ blood_disease ]
|
eng-30-14192376-n
|
inflammatory histiocytosis associated with disturbance of cholesterol metabolism; occurs chiefly in young children and is characterized by cystic defects of the skull and diabetes insipidus
|
+ hematocytopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-13973632-n
|
an abnormally low number of red blood cells in the blood
|
+ hemoglobinopathy
|
n
|
1
|
[ blood_disease ]
|
eng-30-14192034-n
|
a blood disease characterized by the presence of abnormal hemoglobins in the blood
|
+ hemolytic_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14165240-n
|
anemia resulting from destruction of erythrocytes
|
+ hemophilia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14170337-n
|
congenital tendency to uncontrolled bleeding; usually affects males and is transmitted from mother to son
|
+ hemophilia_A
|
n
|
1
|
[ blood_disease ]
|
eng-30-14170772-n
|
hemophilia caused by a congenital deficiency of factor VIII; occurs almost exclusively in men
|
+ hemophilia_B
|
n
|
1
|
[ blood_disease ]
|
eng-30-14170987-n
|
a clotting disorder similar to hemophilia A but caused by a congenital deficiency of factor IX
|
+ hemophilic
|
a
|
1
|
[ blood_disease ]
|
eng-30-02850826-a
|
relating to or having hemophilia
|
+ histiocytosis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14192790-n
|
a blood disease characterized by an abnormal multiplication of macrophages
|
+ hydremia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14193421-n
|
blood disorder in which there is excess fluid volume compared with the cell volume of the blood
|
+ hyperchromic_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14165373-n
|
anemia characterized by an increase in the concentration of corpuscular hemoglobin
|
+ hyperchromic_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14165373-n
|
anemia characterized by an increase in the concentration of corpuscular hemoglobin
|
+ hypervolaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14194942-n
|
a blood disorder consisting of an increase in the volume of circulating blood
|
+ hypervolemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14194942-n
|
a blood disorder consisting of an increase in the volume of circulating blood
|
+ hypochromic_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14165544-n
|
anemia characterized by a decrease in the concentration of corpuscular hemoglobin
|
+ hypochromic_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14165544-n
|
anemia characterized by a decrease in the concentration of corpuscular hemoglobin
|
+ hypoplastic_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14165730-n
|
anemia resulting from inadequately functioning bone marrow; can develop into aplastic anemia
|
+ hypoplastic_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14165730-n
|
anemia resulting from inadequately functioning bone marrow; can develop into aplastic anemia
|
+ hypothrombinemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14194690-n
|
a low level of prothrombin (factor II) in the circulating blood; results in long clotting time and poor clot formation and sometimes excessive bleeding; can result from vitamin K deficiency
|
+ hypovolaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14195112-n
|
a blood disorder consisting of a decrease in the volume of circulating blood
|
+ hypovolaemic
|
a
|
1
|
[ blood_disease ]
|
eng-30-02877313-a
|
of or relating to a decrease in the volume of circulating blood
|
+ hypovolemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14195112-n
|
a blood disorder consisting of a decrease in the volume of circulating blood
|
+ hypovolemic
|
a
|
1
|
[ blood_disease ]
|
eng-30-02877313-a
|
of or relating to a decrease in the volume of circulating blood
|
+ idiopathic_thrombocytopenic_purpura
|
n
|
1
|
[ disease blood_disease ]
|
eng-30-14565417-n
|
purpura associated with a reduction in circulating blood platelets which can result from a variety of factors
|
+ iron_deficiency_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14165909-n
|
a form of anemia due to lack of iron in the diet or to iron loss as a result of chronic bleeding
|
+ iron_deficiency_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14165909-n
|
a form of anemia due to lack of iron in the diet or to iron loss as a result of chronic bleeding
|
+ ischaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14166118-n
|
local anemia in a given body part sometimes resulting from vasoconstriction or thrombosis or embolism
|
+ ischaemic
|
a
|
1
|
[ blood_disease ]
|
eng-30-02751733-a
|
relating to or affected by ischemia
|
+ ischaemic_stroke
|
n
|
1
|
[ blood_disease ]
|
eng-30-14166358-n
|
the most common kind of stroke; caused by an interruption in the flow of blood to the brain (as from a clot blocking a blood vessel)
|
+ ischemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14166118-n
|
local anemia in a given body part sometimes resulting from vasoconstriction or thrombosis or embolism
|
+ ischemic
|
a
|
1
|
[ blood_disease ]
|
eng-30-02751733-a
|
relating to or affected by ischemia
|
+ ischemic_stroke
|
n
|
1
|
[ blood_disease ]
|
eng-30-14166358-n
|
the most common kind of stroke; caused by an interruption in the flow of blood to the brain (as from a clot blocking a blood vessel)
|
+ leucocytosis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14196221-n
|
an abnormal increase in the number of white blood cells in the blood as a result of infection (as in leukemia)
|
+ leucopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14196405-n
|
an abnormal lowering of the white blood cell count
|
+ leukocytosis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14196221-n
|
an abnormal increase in the number of white blood cells in the blood as a result of infection (as in leukemia)
|
+ leukopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14196405-n
|
an abnormal lowering of the white blood cell count
|
+ lymphocytopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14196823-n
|
an abnormally small number of lymphocytes in the circulating blood
|
+ lymphocytosis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14196965-n
|
an abnormal increase in the number of lymphocytes in the circulating blood
|
+ lymphopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14196823-n
|
an abnormally small number of lymphocytes in the circulating blood
|
+ macrocytic_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14166968-n
|
anemia in which the average size of erythrocytes is larger than normal
|
+ macrocytic_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14166968-n
|
anemia in which the average size of erythrocytes is larger than normal
|
+ malignant_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14167426-n
|
a chronic progressive anemia of older adults; thought to result from a lack of intrinsic factor (a substance secreted by the stomach that is responsible for the absorption of vitamin B12)
|
+ malignant_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14167426-n
|
a chronic progressive anemia of older adults; thought to result from a lack of intrinsic factor (a substance secreted by the stomach that is responsible for the absorption of vitamin B12)
|
+ megaloblastic_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14167773-n
|
anemia characterized by many large immature and dysfunctional red blood cells (megaloblasts) in the bone marrow; associated with pernicious anemia
|
+ megaloblastic_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14167773-n
|
anemia characterized by many large immature and dysfunctional red blood cells (megaloblasts) in the bone marrow; associated with pernicious anemia
|
+ metaplastic_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14168010-n
|
pernicious anemia in which the various formed elements in the blood are changed
|
+ metaplastic_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14168010-n
|
pernicious anemia in which the various formed elements in the blood are changed
|
+ microcytic_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14167123-n
|
anemia in which the average size of erythrocytes is smaller than normal
|
+ microcytic_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14167123-n
|
anemia in which the average size of erythrocytes is smaller than normal
|
+ microcytosis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14197099-n
|
a blood disorder characterized by the presence of microcytes (abnormally small red blood cells) in the blood; often associated with anemia
|
+ neutropenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14196543-n
|
leukopenia in which the decrease is primarily in number of neutrophils (the chief phagocytic leukocyte)
|
+ nonthrombocytopenic_purpura
|
n
|
1
|
[ blood_disease ]
|
eng-30-14197628-n
|
purpura resulting from a defect in the capillaries caused by bacteria or drugs
|
+ pancytopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-13973769-n
|
an abnormal deficiency in all blood cells (red blood cells and white blood cells and platelets); usually associated with bone marrow tumor or with aplastic anemia
|
+ parasitaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14167298-n
|
a condition in which parasites are present in the blood
|
+ parasitemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14167298-n
|
a condition in which parasites are present in the blood
|
+ peliosis
|
n
|
1
|
[ blood_disease ]
|
eng-30-14197468-n
|
any of several blood diseases causing subcutaneous bleeding
|
+ pernicious_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14167426-n
|
a chronic progressive anemia of older adults; thought to result from a lack of intrinsic factor (a substance secreted by the stomach that is responsible for the absorption of vitamin B12)
|
+ pernicious_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14167426-n
|
a chronic progressive anemia of older adults; thought to result from a lack of intrinsic factor (a substance secreted by the stomach that is responsible for the absorption of vitamin B12)
|
+ polycythemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14197315-n
|
a disorder characterized by an abnormal increase in the number of red blood cells in the blood
|
+ puerperal_fever
|
n
|
1
|
[ blood_disease ]
|
eng-30-14190493-n
|
serious form of septicemia contracted by a woman during childbirth or abortion (usually attributable to unsanitary conditions); formerly widespread but now uncommon
|
+ purpura
|
n
|
1
|
[ blood_disease ]
|
eng-30-14197468-n
|
any of several blood diseases causing subcutaneous bleeding
|
+ purpura_hemorrhagica
|
n
|
1
|
[ disease blood_disease ]
|
eng-30-14565417-n
|
purpura associated with a reduction in circulating blood platelets which can result from a variety of factors
|
+ pyaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14190736-n
|
septicemia caused by pus-forming bacteria being released from an abscess
|
+ pyaemic
|
a
|
1
|
[ blood_disease ]
|
eng-30-03105430-a
|
of or relating to pyemia
|
+ pyemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14190736-n
|
septicemia caused by pus-forming bacteria being released from an abscess
|
+ pyemic
|
a
|
1
|
[ blood_disease ]
|
eng-30-03105430-a
|
of or relating to pyemia
|
+ refractory_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14168176-n
|
any of various anemic conditions that are not successfully treated by any means other than blood transfusions (and that are not associated with another primary disease)
|
+ refractory_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14168176-n
|
any of various anemic conditions that are not successfully treated by any means other than blood transfusions (and that are not associated with another primary disease)
|
+ Schuller-Christian_disease
|
n
|
1
|
[ blood_disease ]
|
eng-30-14192376-n
|
inflammatory histiocytosis associated with disturbance of cholesterol metabolism; occurs chiefly in young children and is characterized by cystic defects of the skull and diabetes insipidus
|
+ septicaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14189837-n
|
invasion of the bloodstream by virulent microorganisms from a focus of infection
|
+ septicemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14189837-n
|
invasion of the bloodstream by virulent microorganisms from a focus of infection
|
+ septicemic
|
a
|
1
|
[ blood_disease ]
|
eng-30-02115187-a
|
characteristic of septicemia
|
+ shipping_fever
|
n
|
1
|
[ disease blood_disease ]
|
eng-30-14272620-n
|
a deadly form of septicemia in cattle and sheep; involves high fever and pneumonia; contracted under conditions of exposure or exhaustion (as often happens when the animals are shipped to market)
|
+ shipping_pneumonia
|
n
|
1
|
[ disease blood_disease ]
|
eng-30-14272620-n
|
a deadly form of septicemia in cattle and sheep; involves high fever and pneumonia; contracted under conditions of exposure or exhaustion (as often happens when the animals are shipped to market)
|
+ sickle-cell_anaemia
|
n
|
1
|
[ congenital_disease blood_disease ]
|
eng-30-14168792-n
|
a congenital form of anemia occurring mostly in blacks; characterized by abnormal blood cells having a crescent shape
|
+ sickle-cell_anemia
|
n
|
1
|
[ congenital_disease blood_disease ]
|
eng-30-14168792-n
|
a congenital form of anemia occurring mostly in blacks; characterized by abnormal blood cells having a crescent shape
|
+ sickle-cell_disease
|
n
|
1
|
[ congenital_disease blood_disease ]
|
eng-30-14168792-n
|
a congenital form of anemia occurring mostly in blacks; characterized by abnormal blood cells having a crescent shape
|
+ sideroblastic_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14168447-n
|
refractory anemia characterized by sideroblasts in the bone marrow
|
+ sideroblastic_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14168447-n
|
refractory anemia characterized by sideroblasts in the bone marrow
|
+ siderochrestic_anaemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14168447-n
|
refractory anemia characterized by sideroblasts in the bone marrow
|
+ siderochrestic_anemia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14168447-n
|
refractory anemia characterized by sideroblasts in the bone marrow
|
+ thrombocytopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14198019-n
|
a blood disease characterized by an abnormally small number of platelets in the blood
|
+ thrombocytopenic_purpura
|
n
|
1
|
[ disease blood_disease ]
|
eng-30-14565417-n
|
purpura associated with a reduction in circulating blood platelets which can result from a variety of factors
|
+ thrombopenia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14198019-n
|
a blood disease characterized by an abnormally small number of platelets in the blood
|
+ TIA
|
n
|
1
|
[ blood_disease ]
|
eng-30-14166589-n
|
brief episode in which the brain gets insufficient blood supply; symptoms depend on the site of the blockage
|
+ toxaemia
|
n
|
2
|
[ blood_disease ]
|
eng-30-14190907-n
|
blood poisoning caused by bacterial toxic substances in the blood
|
+ toxemia
|
n
|
2
|
[ blood_disease ]
|
eng-30-14190907-n
|
blood poisoning caused by bacterial toxic substances in the blood
|
+ transient_ischemic_attack
|
n
|
1
|
[ blood_disease ]
|
eng-30-14166589-n
|
brief episode in which the brain gets insufficient blood supply; symptoms depend on the site of the blockage
|
+ uratemia
|
n
|
1
|
[ blood_disease symptom ]
|
eng-30-14572353-n
|
presence of abnormal amounts of uric acid salts in the blood; symptom of gout
|
+ uricaciduria
|
n
|
1
|
[ blood_disease symptom ]
|
eng-30-14572951-n
|
presence of abnormal amounts of uric acid in the urine; symptom of gout
|
+ vascular_hemophilia
|
n
|
1
|
[ blood_disease ]
|
eng-30-14171176-n
|
a form of hemophilia discovered by Erik von Willebrand; a genetic disorder that is inherited as an autosomal recessive trait; characterized by a deficiency of the coagulation factor and by mucosal bleeding
|
+ von_Willebrand's_disease
|
n
|
1
|
[ blood_disease ]
|
eng-30-14171176-n
|
a form of hemophilia discovered by Erik von Willebrand; a genetic disorder that is inherited as an autosomal recessive trait; characterized by a deficiency of the coagulation factor and by mucosal bleeding
|
+ Werlhof's_disease
|
n
|
1
|
[ disease blood_disease ]
|
eng-30-14565417-n
|
purpura associated with a reduction in circulating blood platelets which can result from a variety of factors
|