| SCD | 1) Sickle Cell Disease 2) Subacute Combined Degeneration |
|---|---|
| SCID | Severe Combined Immuno-Deficiency; 중증 복합 면역 결핍증 |
| CAH | chronic active hepatitis; chronic aggressive hepatitis; combined atrial hypertrophy; congenital adre... |
| CCT | carotid compression tomography; central conduction time; cerebrocranial trauma; chocolate-coated tab... |
| CDT | carbohydrate-deficient transferrin; carbon dioxide therapy; Certified Dental Technician; children's ... |
| congenital severe combined immunodeficiency | Disease, one form of which is caused by the lack of a transcription factor required for expression of HLA class II genes. (18 Nov 1997) |
|---|---|
| contraceptives, oral, combined | Fixed drug combinations administered orally for contraceptive purposes. (12 Dec 1998) |
| severe combined immunodeficiency | Group of rare congenital disorders characterised by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an x-linked or autosomal recessive defect. About half of the patients with autosomal recessive scid are deficient in the enzyme adenosine deaminase. (12 Dec 1998) |
| severe combined immunodeficient mice | Mice that lack both T and B lymphocytes and are used for transplantation and study of human lymphoid tissues resulting in a SCID-human mouse chimera. See: severe combined immunodeficiency. (05 Mar 2000) |
| 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) |
| 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) |
| Alzheimer's sclerosis | Hyaline degeneration of the medium and smaller blood vessels of the brain. (05 Mar 2000) |
| amyotrophic lateral sclerosis | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
| amyotropic lateral sclerosis | A chronic progressive disease of motor neurons (the nerves that come from the spinal cord to supply electrical energy to the muscles). (12 Dec 1998) |
| arterial sclerosis | <cardiology, disease> Imprecise term for various disorders of arteries, particularly hardening due to fibrosis or calcium deposition, often used as a synonym for atherosclerosis. (17 Oct 1997) |
| arteriocapillary sclerosis | Arteriosclerosis, especially of the finer vessels. (05 Mar 2000) |
| arteriolar sclerosis | <cardiology, disease> Sclerosis and thickening of the walls of the smaller arteries (arterioles). Hyaline arteriolosclerosis, in which there is homogeneous pink hyaline thickening of the arteriolar walls, is associated with benign nephrosclerosis. Hyperplastic arteriolosclerosis, in which there is a concentric thickening with progressive narrowing of the lumina may be associated with malignant hypertension, nephrosclerosis and scleroderma. (17 Oct 1997) |