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  • idiopathic pulmonary hemosiderosis
    Ư¹ß¼º ÆóÇ÷öÁõ(¡­øËúìôÑñø).
  • idiopathic pulmonary hemosiderosis
    Ư¹ß¼º ÆóÇ÷öÁõ
  • idiopathic resorption of tooth
    Ư¹ß¼º Ä¡¾ÆÈí ¼ö(¡­öÍä³ýåâ¥).
  • idiopathic respiratory distress
    Ư¹ß¼º È£Èí°ï¶õ.
  • idiopathic respiratory distress of newborn infant =IRDNI
    ½Å»ý¾ÆÆ¯¹ß¼º È£Èí°ï¶õÁõ.
  • idiopathic respiratory distress syndrome
    Ư¹ß¼º È£Èí°ï¶õÁõÈıº.
  • idiopathic sprue
    Ư¹ß¼º ½ºÇÁ·ç¿ì.
  • idiopathic steatorrhea
    Ư¹ß¼º Áö¹æ¼³»çÁõ(¡­ò·Û¸àÜÞáñø).
  • idiopathic sudden hearing loss
    Ư¹ß¼º µ¹¹ß(¼º)³­Ã»
  • idiopathic systemic fibrosis
    Àü½Å¼º Ư¹ß¼º(îïãóàõ ÷åÛ¡àõ) ¼¶À¯Áõ
  • idiopathic thrombocytopenic purpura
    Ư¹ß¼ºÇ÷¼ÒÆÇ°¨¼Ò¼ºÀڹݺ´(¡­úìá³÷ùÊõá´àõí¹ÚèÜ»)
  • idiopathic thrombocytopenic purpura =ITP
    Ư¹ß¼º Ç÷¼ÒÆÇ °¨¼Ò¼º Àڹݺ´.
  • idiopathic unilateral hyperlucent lung
    Ư¹ß¼º ÀÏÃø¼º °úÅõ°ú¼ºÆó
  • idiopathic uveitis
    Ư¹ß¼ºÆ÷µµ¸·¿°.
  • progressive idiopathic atrophoderma
    ÁøÇ༺ ¿øÀÎºÒ¸í¼º ÇǺΠÀ§ÃàÁõ
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  • idiopathic esophaegal dilatation
    Ư¹ß¼º ½ÄµµÈ®Àå(Áõ).
  • idiopathic esophageal achalasia
    Ư¹ß¼º ½Äµµ°æ·ÃÁõ.
  • idiopathic esophageal achalasia
    Ư¹ß¼º ½Äµµ°æ·ÃÁõ
  • idiopathic esophageal dilatation
    Ư¹ß¼º ½ÄµµÈ®Àå(Áõ).
  • idiopathic facial paralysis
    Ư¹ß¼º ¾È¸é½Å°æ¸¶ºñ.
  • idiopathic facial paralysis
    Ư¹ß¼º ¾È¸é½Å°æ¸¶ºñ
  • idiopathic familial fibromatosis
    Ư¹ß¼º °¡Á·¼º ¼¶À¯Á¾Áõ.
  • idiopathic familial fibromatosis
    Ư¹ß¼º °¡Á·¼º ¼¶À¯Á¾Áõ
  • idiopathic hemochromatosis
    Ư¹ß¼º Ç÷ö ¼ÒÁõ.
  • idiopathic hemorrhagic sarcoma
    Ư¹ß¼º ÃâÇ÷¼º À°Á¾
  • idiopathic hypercalciuria
    Ư¹ß¼º °íÄ®½· ´¢(Áõ).
  • idiopathic hyperkinetic heart syndrome
    Ư¹ß¼º °ú¿îµ¿¼º ½ÉÁõÈıº.
  • idiopathic hypertrophic osteoarthropathy
    Ư¹ß¼º °úÇü¼º °ñ°üÀýº´Áõ.
  • idiopathic hypertrophic osteoarthropathy
    Ư¹ß¼º °ñ ´Ù°øÁõ(÷åÛ¡àõÍéÒýÍîñø), Ư¹ß¼º °ñ Á¶¼ÛÁõ(÷åÛ¡àõÍéðØáçñø), Ư¹ß¼º °úÇü¼º °ñ°üÀýº´Áõ.
  • idiopathic hypertrophic subaortic stenosis
    Ư¹ß¼º ºñÈļº ´ëµ¿¸ÆÆÇ ÇϺÎÇùÂø(Áõ).
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ICL Idiopathic CD4 + T Lymphocytopenia
IGHD Idiopathic Growth Hormone Deficiency
IMDS Idiopathic Myelo-Dysplastic Syndrome
  = Preleukemia
  = Refractory Anemi...
IPF Idiopathic Pulmonary Fibrosis
ITP Idiopathic(Immune) Thrombocytopenic Purpura
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IMN Idiopathic Membranous Nephropathy
IMF Idiopathic Myelofibrosis
IPD Idiopathic Parkinson's disease
IPH Idiopathic Portal Hypertension
IPH Idiopathic pulmonary haemosiderosis
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idiopathic roseola Roseola not occurring as a symptom of a recognised general disease.
(05 Mar 2000)
idiopathic thrombocytopenia purpura <haematology> A rare autoimmune disorder characterised by an acute shortage of platelets with resultant bruising and spontaneous bleeding.
The platelet count becomes exceedingly low and spontaneous bleeding from the gums, gastrointestinal tract and nose can be seen. Physical examination may demonstrate enlargement of the spleen. A typical rash occurs to do microscopic haemorrhage of small blood vessels in the skin.
Platelet counts under 10,000 can lead to spontaneous haemorrhage into the brain causing death. Treatment with corticosteroids is generally effective. Surgical removal of the spleen (splenectomy) is reserved for some patients.
Anti-platelet antibodies are detectable in some cases. It may present in either an acute or a chronic form.
Acronym: ITP
(20 Sep 2002)
idiopathic thrombocytopenic purpura <haematology> A rare autoimmune disorder characterised by an acute shortage of platelets with resultant bruising and spontaneous bleeding.
The platelet count becomes exceedingly low and spontaneous bleeding from the gums, gastrointestinal tract and nose can be seen. Physical examination may demonstrate enlargement of the spleen. A typical rash occurs to do microscopic haemorrhage of small blood vessels in the skin.
Platelet counts under 10,000 can lead to spontaneous haemorrhage into the brain causing death. Treatment with corticosteroids is generally effective. Surgical removal of the spleen (splenectomy) is reserved for some patients.
Anti-platelet antibodies are detectable in some cases. It may present in either an acute or a chronic form.
Acronym: ITP
(20 Sep 2002)
dystonia, idiopathic torsion A form of dystonia known as early-onset torsion dystonia (also called generalised torsion dystonia) begins in childhood around the age of 12. Symptoms typically start in one part of the body, usually in an arm or leg, and eventually spread to the rest of the body within about 5 years. Early-onset torsion dystonia is not fatal, but it can be severely debilitating.
(12 Dec 1998)
t-lymphocytopenia, idiopathic CD4-positive Reproducible depletion of CD4+ lymphocytes below 300 per cubic millimeter in the absence of HIV infection or other known causes of immunodeficiency. This is a rare, heterogeneous syndrome and does not appear to be caused by a transmissible agent.
(12 Dec 1998)
jaundice, chronic idiopathic A familial chronic form of nonhemolytic jaundice thought to be due to a defect in the excretion of conjugated bilirubin and certain other organic anions (e.g., sulfobromophthalein) by the liver. It is characterised by the presence of a brown, coarsely granular pigment in the hepatic cells, which is pathognomonic of the condition.
(12 Dec 1998)
Leber's idiopathic stellate neuroretinitis A unilateral neuroretinitis with perifoveal exudates in Henle's nerve fibre layer producing a macular star and spontaneous regression in a few months.
Synonym: Leber's idiopathic stellate neuroretinitis.
(05 Mar 2000)
Leber's idiopathic stellate retinopathy An inflammation affecting the optic nerve head and the posterior pole of the retina, with cells in the nearby vitreous, usually producing a macular star.
Synonym: papilloretinitis.
(05 Mar 2000)
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