serw-MX  [xml]  
 


    
 Categorias DeCS

C10 Nervous System Diseases .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C10.597.606.643.455 Mental Retardation, X-Linked .
C10.597.606.643.455.937 Rett 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 .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.500 Mental Retardation, X-Linked .
C16.320.322.500.937 Rett Syndrome .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.525 Mental Retardation, X-Linked .
C16.320.400.525.937 Rett Syndrome .
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 .
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
 
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
 
Syndrome .
Symptom Cluster .
Cluster, Symptom .
Clusters, Symptom .
Symptom Clusters .
Syndromes .
0.68
 
Rett Syndrome .
Autism, Dementia, Ataxia, and Loss of Purposeful Hand Use .
Rett Disorder .
Rett's Disorder .
Rett's Syndrome .
Autism Dementia Ataxia Loss of Purposeful Hand Use Syndrome .
Cerebroatrophic Hyperammonemias .
Hyperammonemia, Cerebroatrophic .
Hyperammonemias, Cerebroatrophic .
Retts Syndrome .
Syndrome, Rett .
Syndrome, Rett's .
Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome .
Cerebroatrophic Hyperammonemia .
0.56