serw-MX  [xml]  
 


    
 Categorias DeCS

C05 Musculoskeletal Diseases .
C05.550 Joint Diseases .
C05.550.150 Arthrogryposis .
C05.651 Muscular Diseases .
C05.651.102 Arthrogryposis .
C05.660 Musculoskeletal Abnormalities .
C05.660.077 Arthrogryposis .
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 .
C16.131.621 Musculoskeletal Abnormalities .
C16.131.621.077 Arthrogryposis .
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 .
C18.452.648 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 .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
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 .
1.00
14526
 
Arthrogryposis .
Arthrogryposis Multiplex Congenita .
Arthrogryposis Multiplex Congenita (AMC) .
Congenital Arthromyodysplasia .
Congenital Multiple Arthrogryposis .
Fibrous Ankylosis of Multiple Joints .
Guérin-Stern Syndrome .
Otto Syndrome .
Rocher-Sheldon Syndrome .
Rossi Syndrome .
Arthrogryposes .
Arthrogryposes, Congenital Multiple .
Arthrogryposis Multiplex Congenitas .
Arthrogryposis Multiplex Congenitas (AMC) .
Arthrogryposis, Congenital Multiple .
Arthromyodysplasias, Congenital .
Congenita, Arthrogryposis Multiplex .
Congenita, Arthrogryposis Multiplex (AMC) .
Congenital Arthromyodysplasias .
Congenital Multiple Arthrogryposes .
Congenitas, Arthrogryposis Multiplex .
Congenitas, Arthrogryposis Multiplex (AMC) .
Guerin Stern Syndrome .
Guérin Stern Syndrome .
Multiple Arthrogryposes, Congenital .
Multiple Arthrogryposis, Congenital .
Multiplex Congenita, Arthrogryposis .
Multiplex Congenita, Arthrogryposis (AMC) .
Multiplex Congenitas, Arthrogryposis .
Multiplex Congenitas, Arthrogryposis (AMC) .
Rocher Sheldon Syndrome .
Syndrome, Guerin-Stern .
Syndrome, Guérin-Stern .
Syndrome, Otto .
Syndrome, Rocher-Sheldon .
Syndrome, Rossi .
Amyoplasia Congenita .
Arthromyodysplasia, Congenital .
Myodystrophia Fetalis Deformans .
Guerin-Stern Syndrome .
0.43
701592