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"hereditary deafness and nephropathy"¿¡ ´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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  • ¿µ¹®
    ÇѱÛ
  • music deafness
    À½Ä¡
  • noise deafness
    ¼ÒÀ½³­Ã»
  • occupational deafness
    Á÷¾÷³­Ã»
  • organic deafness
    ±âÁú³­Ã»
  • perceptive deafness
    °¨À½³­Ã»
  • pocket handkerchief deafness
    ¿ª±â·ù³­Ã», ÄÚÇ®À½³­Ã»
  • progressive deafness
    ÁøÇ೭û
  • pure word deafness
    ¼ø¼ö¸»±Í¸ÔÀ½, ¼ø¼ö¾î³ó
  • retrocochlear deafness
    ´ÞÆØÀÌÀÌÈij­Ã»
  • senile deafness
    ³ëÀγ­Ã»
  • sensory deafness
    °¨°¢³­Ã»
  • tone deafness
    À½Ä¡
  • total deafness
    ¿ÏÀü±Í¸ÔÀ½
  • toxic deafness
    µ¶¼º³­Ã»
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  • ¿µ¹®
    ÇѱÛ
  • hereditary edema
    À¯Àü¼º ºÎÁ¾.
  • hereditary edema
    À¯Àü¼º ºÎÁ¾
  • hereditary effect
    À¯ÀüÀû¿µÇâ
  • hereditary elliptocytosis
    À¯Àü¼ºÅ¸¿ø±¸Áõ
  • hereditary enamel hypoplasia
    À¯Àü¼º ¹ý³¶ Áú ÀúÇü¼ºÁõ.
  • hereditary epilepsy
    À¯Àü¼º °£Áú(¡­ÊÖòð).
  • hereditary fragility of bone
    À¯Àü¼º °ñ Ãë¾àÁõ (¡­Íéöªå°ñø).
  • hereditary fragility of bone
    À¯Àü¼º °ñÃë¾àÁõ (¡­Íéöªå°ñø).
  • hereditary fructose intolerance
    À¯Àü¼º ÇÁ·èÅä¿À½º ºÒ³»Áõ(¡­ÝÕÒ±ñø).
  • 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.
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  • total deafness
    (¿Ï)Àü³ó
  • toxic deafness
    Áßµ¶¼º³­Ã»
  • transmission deafness
    ÀüÀ½¼º³ó
  • unilateral deafness
    ÆíÃø³ó, ÀÏÃø³ó
  • unilateral deafness
    ÆíÃø³ó(ø¶ö°Öì), ÀÏÃø³ó
  • congenital hereditary sensorineural
    ¼±Ãµ(¼º) À¯Àü°¨°¢½Å°æ(¼º)
  • exostosis,hereditary multiple
    ´Ù¹ß¼º À¯Àü¼º
  • familial hereditary tremor
    °¡Á·¼º À¯ÀüÁøÀü(Ê«ðéàõë¶îîòèïµ).
  • hearing loss, congenital hereditary
    ¼±Ãµ(¼º) À¯Àü¼º ³­Ã»
  • hereditary
    À¯Àü¼ºÀÇ
  • hereditary adrenogenital syndrome
    À¯Àü¼º ºÎ½Å¼º±â¼º ÁõÈıº.
  • hereditary angioedema
    À¯Àü¼º ¸Æ°üºÎÁ¾
  • hereditary angioedema
    À¯Àü¼ºÇ÷°üºÎÁ¾
  • hereditary aphasia
    À¯Àü(¼º) ½Ç¾î(Áõ).
  • hereditary ataxia
    À¯Àü(¼º) ¿îµ¿½ÇÁ¶.
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MN a blood group in the MNSs blood group system; malignant nephrosclerosis; Master of Nursing; meganewt...
OASD ocular albinism-sensorineural deafness [syndrome]
TBMN thin basement membrane nephropathy
TIN tubulointerstitial nephropathy
TMN thin membrane nephropathy
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 7
HHT Hereditary Haemorrhagic Telangiectasia
HHT1 Hereditary Haemorrhagic Telangiectasia Type 1
HME Hereditary Multiple Exostoses
HNA Hereditary Neuralgic Amyotrophy
HNPP Hereditary Neuropathy with Liability to Pressure Palsies
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    ¼³¸í
  • right and left laterotrusive movement
    Á¿ì Ãø¹æ ¿îµ¿
  • right and left margin of uterus
    ¿À¸¥, ¿Þ Àڱà °¡ÀåÀÚ¸®
  • safety regulation and standard
    ¾ÈÀü Á¶Àý ¹× Ç¥ÁØ
  • salt and pepper appearance
    ¼Ò±Ý ÈÄÃß°¡·ç ¸ð¾ç
  • scalel handles and blade
    ¿Ü°ú¿ë Ä®
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  • separation of child and parents
    Áø·á ÁßÀÇ ¸ðÀÚ ºÐ¸®
  • signs and symptoms
    ¡ÈÄ¿Í Áõ»ó
  • spatial and temporal
    ½Ã°ø
  • subepithelial deposit and sclerosis
    »óÇÇÇÏ ÃàÀû°ú °æÈ­
  • superior and inferior lobe
    »ó ¹× ÇÏ¿±
  • supportive and symptomatic therapy
    Áõ»ó ¿ä¹ý
  • synovial bursae and sheaths
    À±È° ÁÖ¸Ó´Ï ¹× À±È°Áý
  • through-and-through drain
    °üÅë ¹è³ó°ü
  • to and fro absorbent system
    ¿Õº¹ Èí¼ö¹ý
  • to and fro flow
    ÀüÈÄ À¯µ¿
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 7
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)
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)
abstracting and indexing Shortening or summarizing of documents; assigning of descriptors for referencing documents.
(12 Dec 1998)
academies and institutes Organizations representing specialised fields which are accepted as authoritative; may be non-governmental, university or an independent research organization, e.g., national academy of sciences, brookings institution, etc.
(12 Dec 1998)
accounts payable and receivable Short-term debt obligations and assets occurring in the regular course of operational transactions.
(12 Dec 1998)
aged, 80 and over A person 80 years of age and older.
(12 Dec 1998)
algae and fungi Algae represent a group of spore-propagating plants, unicellular or undifferentiated into root, stem, and leaf. They include seaweed and many unicellular fresh water plants, most of which contain chlorophyll. They account for about 90% of the earth's photosynthetic activity. Fungi are eukaryotic, heterotrophic organisms that live as saprobes or parasites and include mushrooms, yeasts, smuts, molds, etc. They lack chlorophyll.
(12 Dec 1998)
alkyl and aryl transferases <enzyme> A somewhat heterogeneous class of enzymes that catalyze the transfer of alkyl or related groups (excluding methyl groups).
Registry number: EC 2.5
(12 Dec 1998)
allergy and immunology A medical specialty concerned with the hypersensitivity of the individual to foreign substances and protection from the resultant infection or disorder.
(12 Dec 1998)
alligators and crocodiles Large, long-tailed reptiles, including caimans, of the order loricata.
(12 Dec 1998)
Amine Precursor Uptake and Decarboxylation <pharmacology, physiology> Paracrine cells of which argentaffin cells are an example. Usage of the term APUD is neither helpful nor memorable.
Acronym: APUD
(11 Nov 1997)
amino acids, peptides, and proteins Amino acids and chains of amino acids connected by peptide linkages.
(12 Dec 1998)
Anderson and Goldberger test A test for typhus in which the patient's blood is injected into a guinea pig's peritoneal cavity. In typhus a typical temperature curve will be observed.
(05 Mar 2000)
anniversaries and special events Occasions to commemorate an event or occasions designated for a specific purpose.
(12 Dec 1998)
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    ÇѱÛ
  • mild and bitter
    ´Ü¸À ¾´¸ÀÀÌ ¹Ý¹ÝÀÎ ¸ÆÁÖ
  • milk and water
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  • reach and frequency
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  • reaper and binder
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  • research and development
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  • rest and recuperation
    (º´»çÀÇ)ÈÞ°¡¿Í ÈÞ¾ç
  • rhythm and blues
    ¸®µë ¾Øµå ºí·ç½º(ÈæÀÎ À½¾ÇÀÇ ÀÏÁ¾,rock'n'rollÀÇ ¸ðü)
  • right of visit (and search)
    =RIGHT OF SEARCH
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