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 Categorias DeCS

C01 Bacterial Infections and Mycoses .
C01.252 Bacterial Infections .
C01.252.200 Central Nervous System Bacterial Infections .
C01.252.200.500 Meningitis, Bacterial .
C01.252.200.500.550 Meningitis, Meningococcal .
C01.252.200.500.550.800 Waterhouse-Friderichsen Syndrome .
C01.252.400 Gram-Negative Bacterial Infections .
C01.252.400.625 Neisseriaceae Infections .
C01.252.400.625.549 Meningococcal Infections .
C01.252.400.625.549.449 Meningitis, Meningococcal .
C01.252.400.625.549.449.800 Waterhouse-Friderichsen Syndrome .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.228 Central Nervous System Infections .
C10.228.228.180 Central Nervous System Bacterial Infections .
C10.228.228.180.500 Meningitis, Bacterial .
C10.228.228.180.500.750 Meningitis, Meningococcal .
C10.228.228.180.500.750.500 Waterhouse-Friderichsen Syndrome .
C10.228.614 Meningitis .
C10.228.614.280 Meningitis, Bacterial .
C10.228.614.280.505 Meningitis, Meningococcal .
C10.228.614.280.505.904 Waterhouse-Friderichsen Syndrome .
C10.500 Nervous System Malformations .
C10.500.507 Malformations of Cortical Development .
C10.500.507.450 Malformations of Cortical Development, Group II .
C10.500.507.450.499 Lissencephaly .
C10.500.507.450.499.249 Cobblestone Lissencephaly .
C10.500.507.450.499.249.500 Walker-Warburg Syndrome .
C11 Eye Diseases .
C11.270 Eye Diseases, Hereditary .
C11.270.881 Walker-Warburg Syndrome .
C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.100 Blood Coagulation Disorders .
C15.378.100.802 Purpura .
C15.378.100.802.843 Waterhouse-Friderichsen Syndrome .
C15.378.463 Hemorrhagic Disorders .
C15.378.463.950 Waterhouse-Friderichsen 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 .
C16.131.666 Nervous System Malformations .
C16.131.666.507 Malformations of Cortical Development .
C16.131.666.507.450 Malformations of Cortical Development, Group II .
C16.131.666.507.450.499 Lissencephaly .
C16.131.666.507.450.499.249 Cobblestone Lissencephaly .
C16.131.666.507.450.499.249.500 Walker-Warburg 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 .
C16.320.577 Muscular Dystrophies .
C16.320.577.750 Walker-Warburg 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 .
C19 Endocrine System Diseases .
C19.053 Adrenal Gland Diseases .
C19.053.500 Adrenal Insufficiency .
C19.053.500.740 Waterhouse-Friderichsen Syndrome .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
C23.550.288.500 Syndrome .
C23.550.414 Hemorrhage .
C23.550.414.950 Purpura .
C23.550.414.950.843 Waterhouse-Friderichsen Syndrome .
C23.888 Signs and Symptoms .
C23.888.885 Skin Manifestations .
C23.888.885.687 Purpura .
C23.888.885.687.843 Waterhouse-Friderichsen 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
 
Walker-Warburg Syndrome .
COD-MD Syndrome .
Cerebroocular Dysplasia-Muscular Dystrophy Syndrome .
Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies, Type A1 .
Fukuyama CMD .
Fukuyama Muscular Dystrophy .
Fukuyama Syndrome .
HARD Syndrome .
Hydrocephalus, Agyria, And Retinal Dysplasia .
LGMD2K .
MDDGA1 .
MEB (Muscle-Eye-Brain) Syndrome .
Muscle Eye Brain Disease .
Muscle-Eye-Brain Disease, POMT1-Related .
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive, With Mental Retardation .
Muscular Dystrophy, Limb-Girdle, Type 2K .
Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies), Type A, 1 .
Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle), Type C, 1 .
Pagon Syndrome .
CMD, Fukuyama .
COD MD Syndrome .
COD-MD Syndromes .
Cerebroocular Dysplasia Muscular Dystrophy Syndrome .
Congenital Muscular Dystrophy Dystroglycanopathy with Brain and Eye Anomalies, Type A1 .
Disease, POMT1-Related Muscle-Eye-Brain .
Diseases, POMT1-Related Muscle-Eye-Brain .
Dystrophy, Fukuyama Muscular .
HARD Syndromes .
Muscle Eye Brain Disease, POMT1 Related .
Muscle-Eye-Brain Diseases .
Muscle-Eye-Brain Diseases, POMT1-Related .
Muscular Dystrophy, Fukuyama .
POMT1-Related Muscle-Eye-Brain Disease .
POMT1-Related Muscle-Eye-Brain Diseases .
Pagon Syndromes .
Syndrome, COD-MD .
Syndrome, Chemke .
Syndrome, Fukuyama .
Syndrome, HARD .
Syndrome, Pagon .
Syndrome, Walker-Warburg .
Syndrome, Warburg .
Syndromes, COD-MD .
Syndromes, HARD .
Syndromes, Pagon .
Walker Warburg Syndrome .
alpha Dystroglycanopathies .
alpha-Dystroglycanopathies .
Cerebromuscular Dystrophy, Fukuyama Type .
Chemke Syndrome .
Fukuyama Congenital Muscular Dystrophy .
Fukuyama Type Congenital Muscular Dystrophy .
Muscle-Eye-Brain Disease .
Muscular Dystrophy, Congenital, Fukuyama Type .
Warburg Syndrome .
0.51
293
 
Syndrome .
Symptom Cluster .
Cluster, Symptom .
Clusters, Symptom .
Symptom Clusters .
Syndromes .
0.38
1445102931
 
Waterhouse-Friderichsen Syndrome .
Meningococcal Waterhouse-Friderichsen Syndrome .
Waterhouse-Friederichsen Syndrome .
Adrenalitides, Meningococcal Hemorrhagic .
Adrenalitis, Meningococcal Hemorrhagic .
Hemorrhagic Adrenalitides, Meningococcal .
Hemorrhagic Adrenalitis, Meningococcal .
Meningococcal Hemorrhagic Adrenalitides .
Meningococcal Waterhouse Friderichsen Syndrome .
Syndrome, Meningococcal Waterhouse-Friderichsen .
Waterhouse Friderichsen Syndrome .
Waterhouse Friederichsen Syndrome .
Waterhouse-Friderichsen Syndrome, Meningococcal .
Fulminant Meningococcal Sepsis with Adrenal Apoplexy .
Meningococcal Hemorrhagic Adrenalitis .
Purpura Fulminans (Waterhouse-Friderichsen Syndrome) .
0.35
14276