| AMC | academic medical center; acetylmethyl carbinol; Animal Medical Center; antibody-mediated cytotoxicit... |
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| XTM | xanthoma tuberosum multiplex |
| AMC | Arthrogryposis Multiplex Congenita |
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| M-FISH | Multiplex-fluorescence in situ hybridization |
| myoclonia | Any disorder characterised by myoclonus. Origin: myo-+ G. Klonos, a tumult Fibrillary myoclonia, the twitching of a limited part or group of fibres of a muscle. Synonym: tetanilla. (05 Mar 2000) |
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| arthrogryposis multiplex congenita | Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000) |
| paramyoclonus multiplex | Synonym: myoclonus multiplex. Origin: para-+ G. Mys, muscle, + klonos, a tumult (05 Mar 2000) |
| mononeuritis multiplex | <endocrinology, neurology> A condition characterised by inflammation of several nerves in unrelated portions of the body, may be seen in association with long-standing diabetes. (27 Sep 1997) |
| myoclonus multiplex | An ill-defined disorder marked by rapid and widespread muscle contractions. Synonym: paramyoclonus multiplex, polyclonia, polymyoclonus. (05 Mar 2000) |
| haemangioendothelioma tuberosum multiplex | An eruption of pinkish papules, caused by hyperplasia of the endothelium of the superficial blood vessels. (05 Mar 2000) |
| xanthoma multiplex | <dermatology, pathology> An accumulation of an excess of lipids in the body due to disturbance of lipid metabolism and marked by the formation of foam cells in skin lesions. (16 Dec 1997) |
| steatocystoma multiplex | Widespread, multiple, thin-walled cysts of the skin that are lined by squamous epithelium, including lobules of sebaceous cells. (05 Mar 2000) |
| dysostosis multiplex | <syndrome> Mucopolysaccharidosis in which there is a deficiency of alpha-l-iduronidase, an accumulation of an abnormal intracellular material, and excretion of dermatan sulfate and heparan sulfate in the urine; with severe abnormality in development of skeletal cartilage and bone, with dwarfism, kyphosis, deformed limbs, limitation of joint motion, spadelike hand, corneal clouding, hepatosplenomegaly, mental retardation, and gargoyle-like facies; autosomal recessive inheritance. See: mucolipidosis. Synonym: dysostosis multiplex, Hurler's disease, lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis. (05 Mar 2000) |
| dysplasia epiphysialis multiplex | A dominantly inherited abnormality of epiphyses characterised by difficulty in walking, pain and stiffness of joints, stubby fingers, and often dwarfism of short-limb type; on X-ray examination, the epiphyses are mottled and irregular; ossification centres are late in appearance and may be multiple, but the vertebrae are normal. There is also an autosomal recessive form . Synonym: dysplasia epiphysialis multiplex. (05 Mar 2000) |
| lymphangioma tuberosum multiplex | A cutaneous lesion characterised by multiple, slightly red, cystlike nodules (located chiefly on the trunk), resulting from fairly large lymphatic vessels and spaces, and groups of proliferating endothelial cells; the lesion has some gross resemblance to spiradenoma, except for the characteristic location. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|