| HED | hereditary ectodermal dysplasia; hydrotropic electron-donor; hypohidrotic ectodermal dysplasia; unit... |
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| HEMPAS | hereditary erythrocytic multinuclearity with positive acidified serum |
| HEMRI | hereditary multifocal relapsing inflammation |
| HEPOD | hereditary expansile polyostotic dysplasia |
| hered | heredity, hereditary |
| autoimmune haemolytic anaemia | <haematology> A condition that results from the cellular destruction (haemolysis) of red blood cells due to antibodies formed to components on the surface of the red blood cells. Origin: Gr. Haima = blood (02 Jan 1998) |
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| Bartonella anaemia | Anaemia occurring in infection with Bartonella bacilliformis and characterised by an acute febrile anaemia of rapid onset and high mortality. Occurs in central Andean mountains of northern South America; vector is phlebotomine sandfly, Lutzomyia. (05 Mar 2000) |
| Belgian Congo anaemia | A form of anaemia occurring in natives of Zaire (formerly the Belgian Congo), with associated oedema of subcutaneous tissues, depigmented regions in the skin, and various gastrointestinal disturbances; thought to result from deficiencies in nutrition. Synonym: Belgian Congo anaemia. (05 Mar 2000) |
| Biermer's anaemia | <haematology> A form of anaemia (low red blood cell counts) that results when the bone marrow fails to produce adequate numbers of red blood cells due to a deficiency in vitamin B12. Intrinsic factor, necessary for normal B12 absorption, may be the underlying cause for B12 deficiency if is not produced in the gastric glands (in the stomach). Origin: Gr. Haima = blood (27 Sep 1997) |
| brickmaker's anaemia | Anaemia associated with hookworm disease. (05 Mar 2000) |
| cameloid anaemia | Anaemia characterised by elliptical erythrocytes (ovalocytes) resembling those observed normally in camels; 1 to 15% of erythrocytes in nonanaemic persons may be oval, but greater proportions are observed in certain patients with microcytic anaemia. See: elliptocytosis. Synonym: cameloid anaemia, ovalocytic anaemia. (05 Mar 2000) |
| macrocytic achylic anaemia | <haematology> A form of anaemia (low red blood cell counts) that results when the bone marrow fails to produce adequate numbers of red blood cells due to a deficiency in vitamin B12. Intrinsic factor, necessary for normal B12 absorption, may be the underlying cause for B12 deficiency if is not produced in the gastric glands (in the stomach). Origin: Gr. Haima = blood (27 Sep 1997) |
| macrocytic anaemia | Any anaemia in which the average size of circulating erythrocytes is greater than normal, i.e., the mean corpuscular volume is 94 cu um or more (normal range, 82 to 92 cu um), including such syndromes as pernicious anaemia, sprue, coeliac disease, macrocytic anaemia of pregnancy, anaemia of diphyllobothriasis, and others. Synonym: megalocytic anaemia. (05 Mar 2000) |
| macrocytic anaemia of pregnancy | An anaemia occurring in pregnancy, related to folate deficiency and characterised by a low level of haemoglobin and a reduced number of erythrocytes, which are larger than normal (macrocytes). (05 Mar 2000) |
| macrocytic anaemia tropical | The macrocytic, megaloblastic anaemia of tropical sprue. (05 Mar 2000) |
| radiation anaemia | Hypoplastic anaemia sometimes occurring after high-level acute or low-level chronic exposure to ionizing radiation. (05 Mar 2000) |
| malignant anaemia | <haematology> A form of anaemia (low red blood cell counts) that results when the bone marrow fails to produce adequate numbers of red blood cells due to a deficiency in vitamin B12. Intrinsic factor, necessary for normal B12 absorption, may be the underlying cause for B12 deficiency if is not produced in the gastric glands (in the stomach). Origin: Gr. Haima = blood (27 Sep 1997) |
| Marchiafava-Micheli anaemia | An infrequent disorder with insidious onset (usually in the third or fourth decade) and chronic course, characterised by episodes of haemolytic anaemia, haemoglobinuria (chiefly at night), pallor, icterus or bronzing of the skin, a moderate degree of splenomegaly, and sometimes hepatomegaly; red blood cells are usually macrocytic and vary considerably in size, but there is no evidence of spherocytosis, erythrophagocytosis, or abnormal leukocytes. The disorder is a result of an abnormality of the red cell membrane which makes the red cell unusually sensitive to lysis by complement. Synonym: Marchiafava-Micheli anaemia, Marchiafava-Micheli syndrome. (05 Mar 2000) |
| refractory anaemia | <haematology> A form of myelodysplasia which primarily affects the red cell production by the bone marrow. In some cases the developing red cells show an internal ring of iron granules. These cells are called sideroblasts. Refractory anaemia and refractory anaemia with sideroblasts are the most common forms of myelodysplasia. Origin: Gr. Haima = blood (13 Nov 1997) |
| refractory anaemia with excess blasts | <haematology> A form of myelodysplasia characterised by the build up of immature white blood cells (blasts) in the bone marrow. If the immature cells are particularly numerous it may indicate a chance of transformation to acute leukaemia and the condition is called refractory anaemia with excess blasts in transformation (RAEBt). Acronym: RAEB (13 Nov 1997) |