| SL | sarcolemma; sclerosing leukoencephalopathy; secondary leukemia; segment length; sensation level; sen... |
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| SU | salicyluric acid; secretory unit; sensation unit; solar urticaria; sorbent unit; spectrophotometric ... |
| PS test | Pancreozymin-Secretion test = combined secretin-CCK test |
| SCD | 1) Sickle Cell Disease 2) Subacute Combined Degeneration |
| SCID | Severe Combined Immuno-Deficiency; 중증 복합 면역 결핍증 |
| hyperlipidemia, familial combined | A disorder genetically distinct from the other inherited hyperlipidemias characterised by the type II or type IV lipoprotein pattern (the pattern may change from time to time and the lipid level may be normal at one time and abnormal at another time). (12 Dec 1998) |
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| subacute combined degeneration of the spinal cord | A subacute or chronic disorder of the spinal cord, such as that occurring in certain patients with vitamin B12 deficiency, characterised by a slight to moderate degree of gliosis in association with spongiform degeneration of the posterior and lateral columns. Synonym: combined sclerosis, combined system disease, funicular myelitis, Putnam-Dana syndrome, vitamin B12 neuropathy. (05 Mar 2000) |
| the combined tendinous expansions of the sartorius | Gracilis, and semitendinosus muscles at the medial border of the tuberosity of the tibia. (05 Mar 2000) |
| familial combined hyperlipemia | familial hyperlipoproteinemia |
| familial combined hyperlipidaemia | <biochemistry, endocrinology> Inherited as a defective gene, this disorder is characterised by elevations in serum cholesterol and/or triglycerides. There are often multiple types of lipoproteins (LDL) elevated in one family. This condition is associated with an increased risk of cardiovascular disease. (27 Sep 1997) |