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"optic neuritis, hereditary"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • optic labyrinthine reflex
    ½Ã°¢¹Ì·Î¹Ý»ç
  • sheath of optic nerve
    ½Ã°¢½Å°æÁý, ½Ã½Å°æÃÊ
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  • hereditary macular degeneration
    À¯Àü¼º Ȳ¹Ýº¯¼º(ë¶îîàõüÜÚèܨàõ).
  • hereditary macular dystrophy
    À¯Àü¼ºÈ²¹ÝÀÌ¿µ¾ç(Áõ)
  • hereditary methemoglobinemia
    À¯Àü¼º ¸ÞÆ®Çì¸ð±Û·ÎºóÇ÷Áõ.
  • hereditary methemoglobinemic cyanosis
    À¯Àü¼º ¸ÞÆ®Çì¸ð±Û·ÎºóÇ÷¼º û»öÁõ.
  • hereditary motor and sensory neuropathy
    À¯Àü¼º¿îµ¿ °¨°¢½Å°æº´Áõ
  • hereditary mutilating keratoma
    À¯Àü¼º Àý´Ü °¢È­Á¾
  • hereditary myotonia
    À¯Àü¼º ±Ù±äÀåÁõ.
  • hereditary nephritis
    À¯Àü¼º ½Å¿°.
  • hereditary neurocutaneous angioma
    À¯Àü¼º ½Å°æ ÇǺΠÇ÷°üÁ¾
  • hereditary nigremia
    À¯Àü¼º ÈæÇ÷Áõ.
  • hereditary nonspherocytic hemolytic anemia
    À¯Àü¼º ºñ±¸Çü ÀûÇ÷±¸¼º ¿ëÇ÷¼º ºóÇ÷.
  • hereditary nonspherocytic hemolytic anemia
    À¯Àü¼ººñ±¸»óÀûÇ÷±¸¿ëÇ÷¼ººóÇ÷
  • hereditary opalescent dentine
    À¯Àü¼º À¯¹é»ö»ó¾ÆÁú.
  • hereditary oral mucoepithelial dysplasia
    À¯Àü¼º ±¸°­ Á¡¸· »óÇÇ ÀÌÇü¼º
  • hereditary orotic aciduria
    À¯Àü¼º ¿À·Îƾ»ê´¢Áõ.
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  • hereditary bullous epidermolysis ³ª e.bullosa hereditaria
    À¯Àü¼º Ç¥ÇǼöÆ÷Áõ.
  • hereditary cerebellar ataxia
    À¯Àü¼º ¼Ò³ú¼º ¿îµ¿½ÇÁ¶.
  • hereditary cerebellar sclerosis
    À¯Àü¼º ¼Ò³ú°æÈ­Áõ.
  • hereditary cerebral hemorrhages with amyloidosis(hchwa)
    À¯Àü¼º ³úÃâÇ÷, ¾Æ¹Ð·ÎÀ̵åÁõ¼º
  • hereditary chorea
    À¯Àü(¼º) ¹«µµº´.
  • hereditary coagulation disorder
    À¯Àü¼º ÀÀ °íÀå¾Ö.
  • hereditary coproporphyria
    À¯Àü¼º ÄÚÇÁ·ÎÆ÷ ¸£ÇǸ®¾Æ.
  • hereditary corneal dystrophy
    À¯Àü¼º °¢¸·ÀÌ ¿µ¾çÁõ.
  • hereditary corneal dystrophy
    À¯Àü¼º°¢¸·ÀÌ¿µ¾çÁõ.
  • hereditary craniofacial dysostosis
    À¯Àü¼º µÎ°³¾È¸éÀ̰ñÁõ
  • hereditary craniofacial dysostosis
    À¯Àü¼º µÎ°³¾È¸éÀ̰ñÁõ(¡­ÔéËÏäÔØüì¶Íéñø).
  • hereditary deaf-mutism
    À¯Àü¼º ³ó¾Æ
  • hereditary deafmutism
    À¯Àü¼º ³ó¾Æ (¡­Öìä¯).
  • hereditary deafness
    À¯Àü¼º ³ó¾Æ
  • hereditary deforming chondrodysplasia
    À¯Àü(¼º) º¯Çü¼º ¿¬°ñÀÌÇü¼º(Áõ).
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OG obstetrics and gynecology; occlusogingival; oligodendrocyte; optic ganglion; orange green; orogastri...
ON occipitonuchal; office nurse; onlay; optic nerve; orthopedic nurse; osteonecrosis; osteonectin; over...
ONG optic nerve glioma
OOA outer optic anlage
OR a logical binary relation that is true if any argument is true, and false otherwise; [o]estrogen rec...
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AHO Albright hereditary osteodystrophy
CHED Congenital Hereditary Endothelial Dystrophy
HANE Hereditary Angio Neurotic Edema
HAE Hereditary Angio-Edema
HCSMA Hereditary Canine Spinal Muscular Atrophy
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
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)
oedema, hereditary angioneurotic A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema.
(12 Dec 1998)
telangiectasia, hereditary haemorrhagic An autosomal dominant vascular anomaly characterised by the presence of multiple small telangiectases of the skin, mucous membranes, gastrointestinal tract, and other organs, associated with recurrent episodes of bleeding from affected sites and gross or occult melena.
(12 Dec 1998)
elliptocytosis, hereditary An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.
(12 Dec 1998)
exostoses, multiple hereditary Hereditary disorder transmitted by an autosomal dominant gene and characterised by multiple exostoses (multiple osteochondromas) near the ends of long bones. The genetic abnormality results in a defect in the osteoclastic activity at the metaphyseal ends of the bone during the remodeling process in childhood or early adolescence. The metaphyses develop benign, bony outgrowths often capped by cartilage. A small number undergo neoplastic transformation.
(12 Dec 1998)
eye diseases, hereditary Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.
(12 Dec 1998)
axis, optic <microscopy> The direction, or directions in an anisotropic crystal along which light is not doubly refracted.
(05 Aug 1998)
ganglionic layer of optic nerve <anatomy, nerve> The inner layer of multipolar neurons in the retina consisting of the relatively large neurons that give rise to the fibres of the optic nerve.
Synonym: stratum ganglionare nervi optici.
(05 Mar 2000)
vascular circle of optic nerve <anatomy, nerve> A network of branches of the short ciliary arteries on the sclera around the point of entrance of the optic nerve.
Synonym: circulus vasculosus nervi optici, circulus arteriosus halleri, circulus zinnii, Haller's circle, Zinn's corona, Zinn's vascular circle.
(05 Mar 2000)
glioma of optic chiasm A slow-growing tumour, usually an astrocytoma, of the optic chiasm in children.
(05 Mar 2000)
medial root of optic tract The smaller division of the posterior end of the optic tract that disappears under the medial geniculate body.
Synonym: radix medialis tractus optici.
(05 Mar 2000)
Graves' optic neuropathy Visual dysfunction due to optic nerve compression in Graves' orbitopathy.
(05 Mar 2000)
pigment epithelium of optic retina pigmented part of retina
coloboma of optic nerve <anatomy, nerve> A congenital notch in the formation of the optic nerve, appearing as a craterlike excavation at the optic disk.
(05 Mar 2000)
postlaminar part of optic nerve <anatomy, nerve> The portion of the optic nerve posterior to the lamina cribrosa of the sclera.
Synonym: pars postlaminaris nervi optici.
(05 Mar 2000)
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