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"hereditary progressive arthroophthalmopathy"¿¡ ´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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  • hereditary glycinuria
    À¯Àü¼º ±Û¸®½Å´¢Áõ.
  • hereditary hemorhagic telangiectasia(osler-weber-rendu disease,)
    À¯Àü¼ºÃâÇ÷¼º¸ð¼¼Ç÷°ü È®Àå
  • hereditary hemorrhagic angioma
    À¯Àü(¼º) ÃâÇ÷¼º Ç÷°üÁ¾.
  • hereditary hemorrhagic telangiectasia
    À¯Àü(¼º) ÃâÇ÷¼º ¸ð¼¼(Ç÷)°üÈ®Àå.
  • hereditary hemorrhagic telangiectasia
    À¯Àü¼º ÃâÇ÷ Ç÷°üÈ®Àå
  • hereditary hyposegmentation
    À¯Àü¼º ÀúºÐ ÀýÁõ.
  • hereditary labyrinthine deafness
    À¯Àü¼º ³»À̼º ³­Ã»(¡­Ò®ì¼àõÑñôé).
  • hereditary labyrinthine deafness
    À¯Àü¼º ³»À̼º ³­Ã»
  • hereditary leptocytosis
    À¯Àü¼º Ç¥ÀûÀûÇ÷±¸ Áõ°¡(Áõ).
  • hereditary lymphedema
    À¯Àü¼º¸²ÇÁºÎÁ¾
  • 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
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  • 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).
  • hereditary deforming chondrodysplasia
    À¯Àü(¼º) º¯Çü¼º ¿¬°ñ ÀÌÇü¼º(Áõ)(ë¶îîàõܨû¡àõæãÍéì¶û¡à÷ñø).
  • hereditary dentin hypoplasia
    À¯Àü¼º »ó¾ÆÁú Çü¼ººÎÀü(Áõ)(¡­ßÚä³òõû¡à÷ÝÕîï ñø).
  • hereditary disease
    À¯Àüº´.
  • hereditary disorder
    À¯Àü¼º Àå¾Ö<Áúº´>
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PPV pneumococcal polysaccharide vaccine; porcine parvovirus; positive predictive value; positive pressur...
PRE photoreacting enzyme; physician's report of examination; pigmented retinal epithelium; preplacement ...
PRF partial reinforcement; patient report form; perforin; plasma recognition factor; pontine reticular f...
prog progress, progressive
PRP physiologic rest position; pityriasis rubra pilaris; platelet-rich plasma; polyribosyl ribitol phosp...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 8
HE Hereditary Elliptocytosis
HFI Hereditary Fructose Intolerance
HHT Hereditary Haemorrhagic Telangiectasia
HHT1 Hereditary Haemorrhagic Telangiectasia Type 1
HMSN Hereditary Motor and Sensory Neuropathies
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 2 ÆäÀÌÁö: 8
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)
Leber's hereditary optic atrophy Hereditary degeneration of the optic nerve and papillomacular bundle with resulting rapid loss of central vision, progressive for several weeks, then usually stationary with permanent central scotoma; age of onset is variable, most often in the third decade; more males than females are affected and transmission is cytoplasmic and strictly on the female side. Mutation on the mitochondrial chromosome involved, which presumably interacts with an X-linked mutant. This mechanism may explain the bizarre sex ratio, which differs significantly from one country to another.
(05 Mar 2000)
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