| hereditary persistence of foetal haemoglobin | <haematology> Hereditary persistence of foetal haemoglobin is a genetic condition where adult types of haemoglobin fail to develop and the types of haemoglobin the individual had as a foetus remains present well past the point when they would normally have stopped being produced. (09 Oct 1997) |
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| hereditary progressive arthro-ophthalmopathy | Autosomal dominant arthro-ophthalmopathy associated with progressive multiple dysplasia of the epiphyses, overtubulation of long bones, cleft lip and palate, hypermobility of joints, flattened vertebral bodies, pelvic bone deformities, and deafness. Synonym: Stickler's syndrome. (05 Mar 2000) |
| hereditary pyropoikilocytosis | A rare recessive disorder manifested by severe haemolysis, marked poikilocytosis, and a characteristic sensitivity of the red cells to heat-induced fragmentation in vitro; apparently due to a defect in spectrin self-association. Synonym: hereditary pyropoikilocytosis. (05 Mar 2000) |
| hereditary sensory radicular neuropathy | Neuropathy characterised by the occurrence of severe, relapsing foot ulcerations of neuropathic origin, destruction of terminal digits of feet and hands, and a loss of sensation; autosomal dominant inheritance is associated with onset in the second decade or later. (05 Mar 2000) |
| hereditary spherocytosis | <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane. This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged. Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal. (27 Sep 1997) |
| hereditary spinal ataxia | Sclerosis of the posterior and lateral columns of the spinal cord, occurring in children and marked by ataxia in the lower extremities, extending to the upper, followed by paralysis and contractures; autosomal recessive inheritance. See: spinocerebellar ataxia. Synonym: Friedreich's ataxia, heredotaxia. (05 Mar 2000) |
| hereditary syphilis | Synonym: congenital syphilis. (05 Mar 2000) |
| heredity | 1. <genetics> The genetic transmission of a particular quality or trait from parent to offspring. 2. The genetic constitution of an individual. Origin: L. Hereditas (18 Nov 1997) |
| heredo- | Heredity. Origin: L. Heres, an heir (05 Mar 2000) |
| heredofamilial tremor | A benign tremor inherited as a dominant character; it may be a rapid oscillation resembling that seen in thyrotoxicosis, a coarse tremor during rest and inhibited by a voluntary effort, or one which appears only upon movement. Synonym: benign essential tremor, familial tremor. (05 Mar 2000) |
| heredopathia atactica polyneuritiformis | A genetic disorder of the fatty acid phytanic acid which accumulates and causes a number of progressive problems including polyneuritis (inflammation of numerous nerves), diminishing vision (due to retinitis pigmentosa), and wobbliness (ataxia) caused by damage to the cerebellar portion of the brain (cerebellar ataxia). (12 Dec 1998) |
| heredotaxia | Sclerosis of the posterior and lateral columns of the spinal cord, occurring in children and marked by ataxia in the lower extremities, extending to the upper, followed by paralysis and contractures; autosomal recessive inheritance. See: spinocerebellar ataxia. Synonym: Friedreich's ataxia, heredotaxia. (05 Mar 2000) |
| heredity |
The total sum of genetic information that humans pass on from generation to generation.
출처: https://www5.nationalgeographic.com/genographic/gl...
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| heredity |
The biological similarity of offspring and parents.
출처: helios.bto.ed.ac.uk/bto/glossary/gh.htm
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| hereditary |
Refers to a disease or condition that is passed from parents to child.
출처: www.bdid.com/termsh.htm
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| hereditary spherocytosis |
a hereditary form of anemia characterized by abnormally shaped red blood cells which are spherical and abnormally fragile. The increased fragility of these red blood cells leads to hemolytic anemia (anemia caused by the rupture of red blood cells).
출처: www.nutrabio.com/Definitions/definitions_h.htm
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| hereditary |
Inherited; inborn; referring to the genetic transmission of a trait, condition, or disorder from parent to offspring.
출처: www.dbs-stn.org/glossary1.asp
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