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  • autonomic nervous system
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  • autonomic imbalance
    ÀÚÀ²½Å°æ ÆòÇüÀÌ»ó(í»ëÏãêÌè øÁû¬ì¶ßÑ).
  • autonomic instability
    ÀÚÀ²½Å°æºÒ¾ÈÁõ.
  • autonomic instability
    ÀÚÀ²½Å°æ ºÒ¾ÈÁõ(í»ëÏãêÌè ÝÕäÌñø)
  • autonomic insufficiency
    ÀÚÀ²½Å°æºÎÀü.
  • autonomic insufficiency
    ÀÚÀ²½Å°æ ºÎÀü(í»ëÏãêÌè Üôîï).
  • autonomic movement
    ÀÚÀ²¼º ¿îµ¿, ÀÚ¹ß ¿îµ¿
  • autonomic nerve
    ÀÚÀ²½Å°æ
  • autonomic nerve fiber
    ÀÚÀ²½Å°æ¼¶À¯
  • autonomic nerve plexus
    ÀÚÀ²½Å°æ¾ó±â
  • autonomic nervous system
    ÀÚÀ²½Å°æ°èÅë, ÀÚÀ²½Å°æ°è(í»ëÏãêÌèͧ).
  • autonomic nervous system
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  • autonomic nervous system
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  • autonomic nervous system
    ÀÚÀ²½Å°æ°è(í»×ÈãêÌèͧ)
  • autonomic neuron
    ÀÚÀ²½Å°æ¼¼Æ÷
  • autonomic plexus
    ÀÚÀ²½Å°æ¾ó±â
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ACEDS angiotensin-converting enzyme dysfunction syndrome
ARC accelerating rate calorimetry; acquired immunodeficiency syndrome-related complex; active renin conc...
AVND atrioventricular node dysfunction
CHD Chediak-Higashi disease; childhood disease; chronic hemodialysis; congenital or congestive heart dis...
CPD calcium pyrophosphate deposition; cephalopelvic disproportion; cerebelloparenchymal disorder; childh...
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LVSD Left ventricular systolic dysfunction
MGD Meibomian gland dysfunction
MBD Minimal Brain Dysfunction
MND Minor neurological dysfunction
MODS Multi Organ Dysfunction Syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 7 ÆäÀÌÁö: 4
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  • familial hypophosphatemic rickets

    familial leiomyomatosis cutis et uteri (°¡Á·¼º ÇǺΠÀڱà ±ÙÁ¾Áõ

  • familial Mediterranean fever
    °¡Á·¼º ÁöÁßÇØ ¿­
  • familial neutropenia
    °¡Á·¼º È£Áß±¸ °¨¼ÒÁõ
  • familial polyposis
    °¡Á·¼º Æú¸³Áõ
  • familial progressive sensorineural hearing loss
    °¡Á·¼º ÁøÇ༺ °¨°¢ ½Å°æ¼º ³­Ã»
  • familial teleangiectasis
    °¡Á·¼º ¸»ÃÊÇ÷°ü È®Àå, °¡Á·¼º ¸»ÃÊÇ÷°ü È®ÀåÁõ
  • fatal familial insomnia
    Ä¡¸íÀû °¡Á·¼º ºÒ¸éÁõ
    ºÒ¸éÁõ°ú ÀÚÀ²½Å°æ Àå¾Ö°¡ ÁÖ Áõ»óÀÌ°í ¸ðµç ȯÀÚ¿¡¼­ PrP À¯ÀüÀÚÀÇ º¯À̸¦ È®ÀÎÇÒ ¼ö ÀÖ´Ù. ÇüÅÂÇÐÀû ¼Ò°ßÀº º¸Åë ½Ã»ó¿¡¼­¸¸ °üÂûµÇ´Âµ¥ ½Å°æ ¼¼Æ÷ÀÇ ¼Ò½Ç°ú ´õºÒ¾î ±³¼¼Æ÷°¡ Áõ½ÄÇϰí ÇØ¸é»ó º¯È­¸¦ º¸ÀδÙ.
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autonomic plexuses Plexus's of nerves in relation to blood vessels and viscera, the component fibres of which are sympathetic, parasympathetic, and sensory.
Synonym: plexus autonomici.
(05 Mar 2000)
ganglia, autonomic Clusters of neurons and their processes in the autonomic nervous system. In the autonomic ganglia, the preganglionic fibres from the central nervous system synapse onto the neurons whose axons are the postganglionic fibres innervating target organs. The ganglia also contain intrinsic neurons and supporting cells and preganglionic fibres passing through to other ganglia.
(12 Dec 1998)
ganglia of autonomic plexuses Autonomic ganglia lying in plexuses of autonomic fibres, e.g., the coeliac and inferior mesenteric ganglia of the sympathetic, and the small parasympathetic ganglia of the myenteric plexus.
Synonym: ganglia plexuum autonomicorum.
(05 Mar 2000)
gastric plexuses of autonomic system The plexus's along the greater and lesser curvatures of the stomach derived from the coeliac plexus; also known as inferior and superior plexus.
Synonym: plexus gastrici systematis autonomici.
(05 Mar 2000)
pulmonary branch of autonomic nervous system Pulmonary branches of cardiac plexuses and cardiaopulmonary splanchnic nerves.
Synonym: rami pulmonales systematis autonomici.
(05 Mar 2000)
nervous system, autonomic Part of the nervous system once thought functionally independent of the brain. The autonomic nervous system regulates key functions including the activity of the cardiac (heart) muscle, smooth muscles (e.g., of the gut), and glands. The autonomic nervous system has two divisions: (1) the sympathetic nervous system, which accelerates the heart rate, constricts blood vessels, and raises blood pressure; and (2) the parasympathetic nervous system, which slows the heart rate, increases intestinal and gland activity, and relaxes sphincter muscles.
(12 Dec 1998)
neuropathies, hereditary sensory and autonomic A group of inherited disorders in which there is selective involvement of the peripheral sensory and autonomic neurons and degeneration of fibres by axonal atrophy and degeneration. Five types of disorders have been described and classified type I through type v.
(12 Dec 1998)
benign familial chorea A rare, nonprogressive movement disorder characterised by chorea and athetosis appearing in early childhood, most commonly manifested as gait ataxia and upper limb coordination. Intellect is unaffected. Probably autosomal-dominance inheritance with incomplete penetrance.
(05 Mar 2000)
benign familial chronic pemphigus Recurrent eruption of vesicles and bullae that become scaling and crusted lesions with vesicular borders, predominantly of the neck, groin, and axillary regions; autosomal dominant inheritance, presenting in late adolescence or early adult life.
Synonym: Hailey-Hailey disease.
(05 Mar 2000)
benign familial icterus Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin.
Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease.
(05 Mar 2000)
cancer, breast, familial A number of factors have been identified that increase the risk of breast cancer. One of the strongest of these risk factors is the history of breast cancer in a relative. About 15-20% of women with breast cancer have such a family history of the disease, clearly reflecting the participation of inherited (genetic) components in the development of some breast cancers. Dominant breast cancer suceptibility genes, including BRCA1 and BRCA2, appear responsible for about 5% of all breast cancer.
(12 Dec 1998)
paralysis, familial periodic An autosomal dominant trait marked by recurring attacks of rapidly progressive flaccid paralysis. There are three types: I, associated with a fall in serum potassium levels (hypokalaemic periodic paralysis); II, associated with a rise therein (hyperkalaemic periodic paralysis, called also adynamia episodica hereditaria); and III, with normal levels (normokalaemic periodic paralysis).
(12 Dec 1998)
pemphigus, benign familial Rare hereditary disease characterised by recurrent eruptions of vesicles and bullae mainly on the neck, axillae, and groin. It exhibits autosomal dominant inheritance and is unrelated to pemphigus vulgaris though it closely resembles that disease.
(12 Dec 1998)
chronic familial icterus <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)
chronic familial jaundice <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)
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