| IPH | idiopathic portal hypertension; idiopathic pulmonary hemosiderosis; idiopathic pulmonary hypertensio... |
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| IHSS(= HCMP) | Idiopathic Hypertrophic Subaortic Stenosis = Obstructive Idiopathic Hypertrophic Car... |
| DISH | diffuse idiopathic skeletal hyperostosis; disseminated idiopathic skeletal hyperostosis |
| IF | idiopathic fibroplasia; idiopathic flushing; immersion foot; immunofluorescence; indirect fluorescen... |
| IH | idiopathic hirsutism; idiopathic hypercalciuria; immediate hypersensitivity; incompletely healed; in... |
| AISA | Acquired Idiopathic Sideroblastic Anemia |
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| AIS | Adolescent Idiopathic Scoliosis |
| CIU | Chronic Idiopathic Urticaria |
| CIIP | Chronic idiopathic intestinal pseudo-obstruction |
| DISH | Diffuse Idiopathic Skeletal Hyperostosis |
| idiopathic roseola | Roseola not occurring as a symptom of a recognised general disease. (05 Mar 2000) |
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| roseola | <paediatrics> Also called baby measles. This is a nonserious but common childhood viral infection that starts with a high fever and swollen lymph glands. After 24 hours, the fever breaks and the child develops a red rash on the neck and trunk. (27 Sep 1997) |
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| roseola infantilis | Another name for Roseola. (12 Dec 1998) |
| roseola infantum | The full name for Roseola. (12 Dec 1998) |
| syphilitic roseola | Usually the first eruption of syphilis, occurring 6 to 12 weeks after the initial lesion. Synonym: erythematous syphilid, macular syphilid. (05 Mar 2000) |
| epidemic roseola | <disease, virology> An acute, usually benign, infectious disease caused by a togavirus and most often affecting children and nonimmune young adults, in which the virus enters the respiratory tract via droplet nuclei and spreads to the lymphatic system. It is characterised by a slight cold, sore throat and fever, followed by enlargement of the postauricular, suboccipital and cervical lymph nodes and the appearances of a fine pink rash that begins on the head and spreads to become generalised. Synonym: German measles, rubeola. Origin: L. Rubellus = reddish, ruber = red (17 Dec 1997) |
| acute idiopathic polyneuritis | <neurology, syndrome> Acute infective polyneuritis that results in a form of peripheral neuropathy with temporary loss of movement and sensation due to inflammation of multiple nerves and loss of myelin. The exact cause is unknown but has been associated with an abnormal immune response to viral infection, particularly cytomegalovirus infection, in which there is cell-mediated immunity to a component of myelin. The disease may be autoimmune in origin and complete recovery can take up to six months. Synonym: Guillain-Barre syndrome (12 Jul 2000) |
| chronic idiopathic jaundice | <syndrome> An inherited disorder (autosomal recessive) that is characterised by long-standing mild jaundice. This occurs secondary to an abnormality in the transport of bilirubin from the liver to the biliary system. This leads to an accumulation of bilirubin in the liver. Avoidance of alcohol and medications which can affect the liver is important. Inheritance: autosomal recessive. (27 Sep 1997) |
| chronic idiopathic xanthomatosis | Vague or indefinite term for inherited abnormalities of lipid metabolism leading to xanthoma formation (e.g., primary familial xanthomatosis). (05 Mar 2000) |
| multiple idiopathic haemorrhagic sarcoma | <oncology, tumour> A type of vascular cancer characterised by soft purple nodules that usually develop first on the feet and then slowly spread across the skin.This cancer is most often found in people with compromised immune systems, such as AIDS patients. (09 Oct 1997) |
| primary idiopathic macular atrophy | Atrophoderma in which the skin becomes bag like and wrinkled. Synonym: atrophia maculosa varioliformis cutis, atrophoderma maculatum, macular atrophy, primary idiopathic macular atrophy, primary macular atrophy of skin. Origin: G. Anetos, relaxed, + derma, skin (05 Mar 2000) |
| purpura, thrombocytopenic, idiopathic | Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IgG autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms. (12 Dec 1998) |
| hyperostosis, diffuse idiopathic skeletal | A disease of elderly men characterised by large osteophytes that bridge vertebrae and ossification of ligaments and tendon insertions. (12 Dec 1998) |
| diffuse idiopathic skeletal hyperostosis | A form of degenerative arthritis characteristically associated with flowing calcification along the sides of the vertebrae of the spine and commonly with inflammation (tendinitis) and calcification of the tendons at their attachments points to bone. Because areas of the spine and tendons can become inflamed, antiinflammatory medications (NSAIDs), such ibuprofen, can be helpful in both relieving pain and inflammation. Also called Forestier's disease. (12 Dec 1998) |
| idiopathic | Of the nature of an idiopathy, self originated, of unknown causation. (18 Nov 1997) |
| idiopathic aldosteronism | An adrenocortical disorder caused by excessive secretion of aldosterone and characterised by headaches, nocturia, polyuria, fatigue, hypertension, potassium depletion, hypokalaemic alkalosis, hypervolaemia, and decreased plasma renin activity; may be associated with small benign adrenocortical adenomas. Synonym: Conn's syndrome, idiopathic aldosteronism. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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