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Startle Syndromes CID10 - Classificação Internacional de Doenças DeCS Português DeCS Inglês DeCS Espanhol DeCS Espanha DeCS Português com escopo DeCS Inglês com escopo DeCS Espanhol com escopo DeCS Espanha com escopo LILACS - LILACS Regional
Categorias DeCS C06 Digestive System Diseases . C06.405 Gastrointestinal Diseases . C06.405.469 Intestinal Diseases . C06.405.469.637 Malabsorption Syndromes . C06.405.469.637.145 Blind Loop Syndrome . C10 Nervous System Diseases . C10.114 Autoimmune Diseases of the Nervous System . C10.114.812 Stiff-Person Syndrome . C10.228 Central Nervous System Diseases . C10.228.854 Spinal Cord Diseases . C10.228.854.790 Stiff-Person Syndrome . C10.668 Neuromuscular Diseases . C10.668.900 Stiff-Person Syndrome . C14 Cardiovascular Diseases . C14.907 Vascular Diseases . C14.907.355 Embolism and Thrombosis . C14.907.355.830 Thrombosis . C14.907.355.830.925 Venous Thrombosis . C14.907.355.830.925.462 Postthrombotic Syndrome . C14.907.952 Venous Insufficiency . C14.907.952.880 Postthrombotic Syndrome . C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities . C16.131 Congenital Abnormalities . C16.131.077 Abnormalities, Multiple . C16.131.077.860 Smith-Lemli-Opitz Syndrome . C16.320 Genetic Diseases, Inborn . C16.320.565 Metabolism, Inborn Errors . C16.320.565.398 Lipid Metabolism, Inborn Errors . C16.320.565.398.850 Smith-Lemli-Opitz Syndrome . C16.320.565.925 Steroid Metabolism, Inborn Errors . C16.320.565.925.875 Smith-Lemli-Opitz Syndrome . C18 Nutritional and Metabolic Diseases . C18.452 Metabolic Diseases . C18.452.584 Lipid Metabolism Disorders . C18.452.584.500 Dyslipidemias . C18.452.584.500.937 Smith-Lemli-Opitz Syndrome . C18.452.603 Malabsorption Syndromes . C18.452.603.145 Blind Loop Syndrome . C18.452.648 Metabolism, Inborn Errors . C18.452.648.398 Lipid Metabolism, Inborn Errors . C18.452.648.398.850 Smith-Lemli-Opitz Syndrome . C18.452.648.925 Steroid Metabolism, Inborn Errors . C18.452.648.925.875 Smith-Lemli-Opitz Syndrome . C20 Immune System Diseases . C20.111 Autoimmune Diseases . C20.111.258 Autoimmune Diseases of the Nervous System . C20.111.258.850 Stiff-Person Syndrome . C23 Pathological Conditions, Signs and Symptoms . C23.550 Pathologic Processes . C23.550.288 Disease . C23.550.288.500 Syndrome .		Termos  Sinônimos e Históricos Documentos LILACS e MDL   Stiff-Person Syndrome . Congenital Stiff-Man Syndrome . Congenital Stiff-Person Syndrome . Familial Hyperekplexia . Hereditary Hyperekplexia . Startle Syndrome . Stiff-Baby Syndrome . Stiff-Trunk Syndrome . Stiffman Syndrome . Congenital Stiff Man Syndrome . Congenital Stiff-Man Syndromes . Congenital Stiff-Person Syndromes . Familial Hyperekplexias . Hereditary Hyperekplexias . Hyperekplexia, Familial . Hyperekplexia, Hereditary . Hyperekplexias, Familial . Hyperekplexias, Hereditary . Moersch Woltmann Syndrome . Startle Syndromes . Stiff Man Syndrome . Stiff Person Syndrome . Stiff Trunk Syndrome . Stiff-Baby Syndromes . Stiff-Man Syndrome, Congenital . Stiff-Man Syndromes, Congenital . Stiff-Person Syndrome, Congenital . Stiff-Person Syndromes, Congenital . Stiff-Trunk Syndromes . Syndrome, Congenital Stiff-Man . Syndrome, Congenital Stiff-Person . Syndrome, Moersch-Woltmann . Syndrome, Startle . Syndrome, Stiff-Baby . Syndrome, Stiff-Man . Syndrome, Stiff-Person . Syndrome, Stiff-Trunk . Syndrome, Stiffman . Syndromes, Congenital Stiff-Man . Syndromes, Congenital Stiff-Person . Syndromes, Startle . Syndromes, Stiff-Baby . Syndromes, Stiff-Trunk . Moersch-Woltmann Syndrome . Stiff-Man Syndrome . 1.00   Syndrome . Symptom Cluster . Cluster, Symptom . Clusters, Symptom . Symptom Clusters . Syndromes . 0.68   Blind Loop Syndrome . Bacterial Overgrowth Syndrome . Stagnant Loop Syndrome . Loop Syndrome, Stagnant . Loop Syndromes, Stagnant . Stagnant Loop Syndromes . Syndrome, Bacterial Overgrowth . Syndrome, Blind Loop . Syndrome, Stagnant Loop . Syndromes, Stagnant Loop . 0.59   Postthrombotic Syndrome . Venous Stasis Syndrome . Syndrome, Postthrombotic . Syndrome, Venous Stasis . 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 . 0.57