Mixed Connective Tissue Disease. MCTD 6868 . Syndrome, Sharp . Connective Tissue Disease, Mixed . Sharp Syndrome . A syndrome with overlapping clinical features of systemic lupus erythematosus, scleroderma, polymyositis, and Raynaud's phenomenon. The disease is differentially characterized by high serum titers of antibodies to ribonuclease-sensitive extractable (saline soluble) nuclear antigen and a "speckled" epidermal nuclear staining pattern on direct immunofluorescence. . 1.00
Shaken Baby Syndrome. Brain injuries resulted from vigorous shaking of an infant or young child held by the chest, shoulders, or extremities causing extreme cranial acceleration. It is characterized by the intracranial and intraocular hemorrhages with no evident external trauma. Serious cases may result in death. . 0.60
Sharks. Shark . A group of elongate elasmobranchs. Sharks are mostly marine fish, with certain species large and voracious. . 0.58
Smith-Lemli-Opitz Syndrome. 7-Dehydrocholesterol Reductase Deficiency . Hyperotosis Corticalis Generalisata Familiaris . Lethal Acrodysgenital Syndrome . Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobar Lung . RSH Syndrome . RSH-SLO Syndrome . Rutledge Friedman Harrod Syndrome . Rutledge Lethal Multiple Congenital Anomaly Syndrome . SLO Syndrome . Smith Lemli Opitz syndrome, type 1 . Smith-Lemli-Opitz Syndrome, Type 1 . Smith-Lemli-Opitz Syndrome, Type 2 . Smith-Lemli-Opitz Syndrome, Type I . Smith-Lemli-Opitz Syndrome, Type II . 7-Dehydrocholesterol Reductase Deficiencies . Acrodysgenital Syndrome, Lethal . Acrodysgenital Syndromes, Lethal . Deficiencies, 7-Dehydrocholesterol Reductase . Deficiency, 7-Dehydrocholesterol Reductase . Lethal Acrodysgenital Syndromes . RSH SLO Syndrome . RSH Syndromes . RSH-SLO Syndromes . Reductase Deficiencies, 7-Dehydrocholesterol . Reductase Deficiency, 7-Dehydrocholesterol . SLO Syndromes . Smith Lemli Opitz Syndrome . Smith Lemli Opitz Syndrome, Type 2 . Smith Lemli Opitz Syndrome, Type I . Smith Lemli Opitz Syndrome, Type II . Syndrome, Lethal Acrodysgenital . Syndrome, RSH . Syndrome, SLO . Syndromes, RSH . Syndromes, SLO . An autosomal recessive disorder of CHOLESTEROL metabolism. It is caused by a deficiency of 7-dehydrocholesterol reductase, the enzyme that converts 7-dehydrocholesterol to cholesterol, leading to an abnormally low plasma cholesterol. This syndrome is characterized by multiple CONGENITAL ABNORMALITIES, growth deficiency, and INTELLECTUAL DISABILITY. . 0.57
Scientists for Health and Research for Development. SHARED . Digital network based on validated information on ongoing medical and health related research, researchers and institutions. (http://www.nwo.nl/nwohome.nsf/pages/NWOP_5VDE7Q_Eng) (http://www.eldis.org/go/home&id=3540&type=Organisation#.VTFthNJVhBc) . 0.56
