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"coarctation of aorta, infantile type"¿¡ ´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®
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  • simple type schizophrenia
    ´Ü¼øÇüÁ¤½ÅºÐ¿­º´
  • viral hepatitis type A
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    BÇü¹ÙÀÌ·¯½º°£¿°
  • viral hepatitis type D
    DÇü¹ÙÀÌ·¯½º°£¿°
  • wild type
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  • wild type strain
    ¾ß»ýÁÖ
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  • lepromatous type
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  • leptosomatic type
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  • mating type
    ±³¹èÇü
  • meromyarian type
    ºÎºÐ±ÙÀ°Çü
  • plaque-type mutation
    ÇöóÅ©Çüµ¹¿¬º¯ÀÌ
  • nomenclatural type
    ºÐ·ùÇÐÀû±âÁظí
  • organic reaction type
    ±âÁú¹ÝÀÀÇü
  • ovulatory type
    ¹è¶õÇü
  • parthenogenetic type
    ´Ü¼º»ý½ÄÇü
  • polymyarian type
    ´Ù±ÙÀ°Çü
  • propagative type
    Áõ½ÄÇü
  • pyknic body type
    ºñ¸¸½ÅüÇü
  • split-electrode-type probe
    ºÐÇÒÀü±Ø´õµëÀÚ
  • storage-type
    ÃàÀûÇü
  • scirrhous type
    °æÈ­Çü
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  • hypersensitivity reactions,type iv(cell-mediated)
    IVÇü
  • hypersensitivity, delayed-type
    Áö¿¬Çü °ú¹Î¹ÝÀÀ
  • hypersensitivity, immediate-type
    Áï½ÃÇü °ú¹Î¹ÝÀÀ
  • hypertrophic type
    ºñ´ëÇü
  • hypogammaglobulinemia, Swiss-type
    ½ºÀ§½ºÇü °¨¸¶±Û·ÎºÒ¸°ÀúÇ÷Áõ
  • personality disorder, mixed type
    È¥ÀçÇü(ûèî¤úþ) ÀΰÝÀå¾Ö
  • personality, type A
    AÇü ÀΰÝ
  • personality, type B
    BÇü ÀΰÝ
  • phage type
    ÆÄÁöÇü(¡­úþ).
  • phage type
    ÆÄÁöÇü
  • phased linear array type
    À§»óÂ÷ ¼±Çü ¹è¿­½Ä
  • phased linear array type
    À§»óÂ÷ ¹è¿­½Ä ¼±Çü (êÈßÓó¬ ÛÕÖªãÒ àÊû¡) Æ®·£½ºµà¼­
  • pilus, type 1
    Á¦1Çü ¼¶¸ð
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    ÇöóÅ©Çü µ¹¿¬º¯ÀÌ
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    Ç÷¼ÒÆÇÇü(û¡)
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  • infantile autism
    ¿µ¾ÆÀÚÆó(Áõ)(?ä®í»øÍñø).
  • infantile automatism
    À¯(¿µ)¾ÆÀÚµ¿Áõ,Á¥¸ÔÀÌÀÚµ¿Áõ
  • infantile automatism
    ¿µ¾ÆÀÚµ¿Áõ, Á¥¸ÔÀÌÀÚµ¿Áõ.
  • infantile beriberi
    ¿µ¾Æ°¢±â( ä®ÊÅѨ).
  • infantile beriberi
    ¿µ¾Æ°¢±â(?ä®ÊÅѨ).
  • infantile cataract
    ¿µ¾Æ±â¹é³»Àå
  • infantile cerebral paralysis
    ¿µ¾Æ(¼º) ³ú¼º¸¶ºñ(?ä®àõÒààõØ«Ýö).
  • infantile convulsion
    À¯(¿µ)¾Æ°æ·Ã
  • infantile convulsion
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  • infantile cortical hyperostosis
    ¿µ¾Æ ÇÇÁú¼º °ú°ñÁõ(~ä®ù«òõàõΦÍéñø), ¿µ¾Æ°ñ¸·ÇÇÁúÁõ½ÄÁõ.
  • infantile cortical hyperostosis
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  • infantile dermatitis
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  • infantile dermatitis
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  • infantile diarrhea
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  • infantile diarrhea =summer d.
    ¿µ¾Æ¼³»çÁõ(?ä®àÜÞáñø).
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DA dark adaptation; dark agouti [rat]; daunomycin; degenerative arthritis; delayed action; Dental Assis...
DAo descending aorta
Desc Ao descending aorta
RCS rabbit aorta-contracting substance; red cell suspension; reticulum cell sarcoma; right coronary sinu...
SAS sarcoma amplified sequence; self-rating anxiety scale; short arm splint; Sklar Aphasia Scale; sleep ...
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HSV-2 Herpes Simplex Virus type I and type 2
HIV-2 Human Immunodeficiency Virus type 1 and type 2
HSV 2 herpes simplex virus type 1 or type 2
Type 1 type
type I type B
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CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
infantile pellagra A nutritional deficiency illness in children who are not getting enough protein, this results in anaemia, poor growth, weakness, and oedema (which isparticularly characterised by a pronounced pot belly). Infamine-stricken regions, children typically develop kwashiorkor rightafter they are weaned.
(09 Oct 1997)
infantile progressive spinal muscular atrophy Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised.
Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy.
(05 Mar 2000)
infantile purulent conjunctivitis Acute conjunctival inflammation in the newborn, usually caused by maternal gonococcal infection. The causative agent is neisseria gonorrhoeae. The baby's eyes are contaminated during passage through the birth canal.
(12 Dec 1998)
infantile sexuality In psychoanalytic personality theory, the concept concerning psychosexual development in infants and children; encompasses the overlapping oral, anal, and phallic phases during the first five years of life.
(05 Mar 2000)
infantile spasm Brief (1 to 3 seconds) muscular spasm's in infants with West's syndrome, which often appear as nodding or salaam spasm's.
Synonym: salaam convulsions.
(05 Mar 2000)
infantile spastic paraplegia A spastic paralysis of the lower extremities occurring in the infant.
Synonym: infantile spastic paraplegia.
(05 Mar 2000)
infantile spinal muscular atrophy Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised.
Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy.
(05 Mar 2000)
infantile tetany Tetany of infants occurring usually in rickets, due to dietary deficiency of vitamin D.
(05 Mar 2000)
early infantile autism A severe emotional disturbance of childhood characterised by qualitative impairment in reciprocal social interaction and in communication, language, and social development.
Synonym: autistic disorder, childhood schizophrenia, early infantile autism, Kanner's syndrome.
(05 Mar 2000)
endemic nonbacterial infantile gastroenteritis An endemic viral gastroenteritis of young children (6 months to 12 years) that is especially widespread during winter, caused by strains of rotavirus; the incubation period is 2 to 4 days, with symptoms lasting 3 to 5 days, including abdominal pain, diarrhoea, fever, and vomiting.
Synonym: infantile gastroenteritis.
(05 Mar 2000)
acrocephalosyndactyly type 1 <paediatrics> An inherited disease (autosomal dominant) or a spontaneously occurring disease characterised by a peaked head and unusual facial appearance, due to the premature closure of the cranial sutures.
A skull X-ray can confirm the diagnosis and treatment is surgical.
Inheritance: autosomal dominant.
(27 Sep 1997)
Alzheimer type I astrocyte Enlarged frequently multinucleated astrocytes, seen in progressive multifocal leukoencephalopathy.
(05 Mar 2000)
Alzheimer type II astrocyte Enlarged astrocytes with vesicular nuclei and one or more small basophilic nucleoli, seen in hepatocerebral disease and Wilson's disease.
(05 Mar 2000)
American Type Culture Collection <cell culture> A key resource for cultured cells, located in Rockville, USA.
(12 Dec 1998)
Antoni type A neurilemoma <tumour> Relatively solid or compact arrangement of neoplastic tissue that consists of Schwann cells arranged in twisting bundles and associated with delicate reticulin fibres; the nuclei of the Schwann cells are frequently grouped in parallel rows (so-called palisades), and the nuclei and fibres sometimes form exaggerated tactile corpuscles, called Verocay bodies.
(05 Mar 2000)
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