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 Categorias DeCS

C10 Nervous System Diseases .
C10.177 Autonomic Nervous System Diseases .
C10.177.575 Primary Dysautonomias .
C10.177.575.300 Dysautonomia, Familial .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.228.140.163.100.435.340 Glycogen Storage Disease Type II .
C10.500 Nervous System Malformations .
C10.500.300 Hereditary Sensory and Motor Neuropathy .
C10.500.310 Hereditary Sensory and Autonomic Neuropathies .
C10.500.310.309 Dysautonomia, Familial .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.495 Hereditary Sensory and Motor Neuropathy .
C10.574.500.496 Hereditary Sensory and Autonomic Neuropathies .
C10.574.500.496.250 Dysautonomia, Familial .
C10.668 Neuromuscular Diseases .
C10.668.829 Peripheral Nervous System Diseases .
C10.668.829.800 Polyneuropathies .
C10.668.829.800.175 Hereditary Sensory and Autonomic Neuropathies .
C10.668.829.800.175.250 Dysautonomia, Familial .
C10.668.829.800.300 Hereditary Sensory and Motor Neuropathy .
C14 Cardiovascular Diseases .
C14.240 Cardiovascular Abnormalities .
C14.240.400 Heart Defects, Congenital .
C14.240.400.172 Barth Syndrome .
C14.280 Heart Diseases .
C14.280.400 Heart Defects, Congenital .
C14.280.400.172 Barth Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.121 Barth Syndrome .
C16.131.240 Cardiovascular Abnormalities .
C16.131.240.400 Heart Defects, Congenital .
C16.131.240.400.172 Barth Syndrome .
C16.131.666 Nervous System Malformations .
C16.131.666.300 Hereditary Sensory and Motor Neuropathy .
C16.131.666.310 Hereditary Sensory and Autonomic Neuropathies .
C16.131.666.310.309 Dysautonomia, Familial .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.068 Barth Syndrome .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.375 Hereditary Sensory and Motor Neuropathy .
C16.320.400.415 Hereditary Sensory and Autonomic Neuropathies .
C16.320.400.415.309 Dysautonomia, Familial .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.189.435.340 Glycogen Storage Disease Type II .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.449 Glycogen Storage Disease .
C16.320.565.202.449.500 Glycogen Storage Disease Type II .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.224 Barth Syndrome .
C16.320.565.398.481 Hyperlipoproteinemia Type II .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.340 Glycogen Storage Disease Type II .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.132.100.435.340 Glycogen Storage Disease Type II .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.500 Dyslipidemias .
C18.452.584.500.500 Hyperlipidemias .
C18.452.584.500.500.644 Hyperlipoproteinemias .
C18.452.584.500.500.644.475 Hyperlipoproteinemia Type II .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.340 Glycogen Storage Disease Type II .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.449 Glycogen Storage Disease .
C18.452.648.202.449.500 Glycogen Storage Disease Type II .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.224 Barth Syndrome .
C18.452.648.398.481 Hyperlipoproteinemia Type II .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.340 Glycogen Storage Disease Type II .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Hereditary Sensory and Autonomic Neuropathies .
Acroosteolysis, Giaccai Type .
Acroosteolysis, Neurogenic .
Congenital Insensitivity to Pain with Anhidrosis .
Familial Dysautonomia, Type 2 .
Familial Dysautonomia, Type II .
Giaccai Type Acroosteolysis .
HSAN (Hereditary Sensory Autonomic Neuropathy) .
HSAN 1 .
HSAN 4 .
HSAN 5 .
HSAN I .
HSAN IV .
HSAN V .
HSAN2 .
HSAN5 .
HSANII .
Hereditary Sensory And Autonomic Neuropathy IV .
Hereditary Sensory Autonomic Neuropathy, Type 1 .
Hereditary Sensory Autonomic Neuropathy, Type 2 .
Hereditary Sensory Autonomic Neuropathy, Type 4 .
Hereditary Sensory Autonomic Neuropathy, Type 5 .
Hereditary Sensory Neuropathy Type 1 .
Hereditary Sensory Neuropathy Type I .
Hereditary Sensory Neuropathy Type Ia .
Hereditary Sensory Radicular Neuropathy .
Hereditary Sensory Radicular Neuropathy, Recessive Form .
Hereditary Sensory and Autonomic Neuropathy 4 .
Hereditary Sensory and Autonomic Neuropathy Type 1 .
Hereditary Sensory and Autonomic Neuropathy Type 2 .
Hereditary Sensory and Autonomic Neuropathy Type I .
Hereditary Sensory and Autonomic Neuropathy Type II .
Hereditary Sensory and Autonomic Neuropathy Type IV .
Hereditary Sensory and Autonomic Neuropathy Type V .
Hereditary Sensory and Autonomic Neuropathy, Type 4 .
Hereditary Sensory and Autonomic Neuropathy, Type 5 .
Insensitivity to Pain, Congenital, with Anhidrosis .
Neurogenic Acroosteolysis .
Neuropathy Hereditary Sensory Radicular, Autosomal Dominant .
Neuropathy Hereditary Sensory and Autonomic Type 1 .
Neuropathy, Congenital Sensory .
Neuropathy, Congenital Sensory, with Anhidrosis .
Neuropathy, Hereditary Sensory And Autonomic, Type I .
Neuropathy, Hereditary Sensory And Autonomic, Type V .
Neuropathy, Hereditary Sensory Radicular, Autosomal Dominant .
Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive .
Neuropathy, Hereditary Sensory, Type I .
Neuropathy, Progressive Sensory, Of Children .
Acroosteolyses, Neurogenic .
Congenital Sensory Neuropathies .
Congenital Sensory Neuropathy .
HSANs (Hereditary Sensory Autonomic Neuropathy) .
HSN Type IIs .
Hereditary Sensory Neuropathies .
Hereditary Sensory Neuropathy .
Neurogenic Acroosteolyses .
Neuropathies, Congenital Sensory .
Neuropathies, Hereditary Sensory .
Neuropathy, Hereditary Sensory .
Sensory Neuropathies, Congenital .
Sensory Neuropathies, Hereditary .
Sensory Neuropathy, Congenital .
Type I, HSAN .
Type I, HSN .
Type IV, HSAN .
Neuropathies, Hereditary Sensory and Autonomic .
HSAN 13449 .
HSAN Type I .
HSAN Type II .
HSAN Type IV .
HSAN Type V .
HSN Type I .
HSN Type II .
Sensory and Autonomic Neuropathies, Hereditary .
Sensory Neuropathy, Hereditary .
Insensitivity to Pain with Anhidrosis, Congenital .
Pain Insensitivity with Anhidrosis, Congenital .
1.00
 
Barth Syndrome .
3-Methylglutaconic Aciduria, Type II .
3-Methylglutaconicaciduria Type 2 .
3-Methylglutaconicaciduria Type II .
Cardioskeletal Myopathy with Neutropenia and Abnormal Mitochondria .
MGA Type 2 .
MGA Type II .
3 Methylglutaconic Aciduria, Type II .
3 Methylglutaconicaciduria Type 2 .
3-Methylglutaconicaciduria Type 2s .
3-Methylglutaconicaciduria Type IIs .
MGA Type 2s .
MGA Type IIs .
Syndrome, Barth .
Type 2, 3-Methylglutaconicaciduria .
Type 2, MGA .
Type 2s, MGA .
Type II, MGA .
Type IIs, MGA .
MGA type II .
3-methylglutaconicaciduria type 2 .
3-methylglutaconicaciduria type II .
0.58
 
Hyperlipoproteinemia Type II .
Apolipoprotein B-100, Familial Defective .
Apolipoprotein B-100, Familial Ligand-Defective .
Familial Combined Hyperlipoproteinemia .
Hyper-Low Density Lipoproteinemia .
Hyper-Low-Density-Lipoproteinemia .
Hyper-beta-Lipoproteinemia .
Hypercholesterolemia, Autosomal Dominant .
Hypercholesterolemia, Autosomal Dominant, Type B .
Hypercholesterolemic Xanthomatosis, Familial .
Hyperlipoproteinemia Type 2 .
Hyperlipoproteinemia Type IIa .
Hyperlipoproteinemia Type IIb .
Hyperlipoproteinemia, Type II .
Hyperlipoproteinemia, Type IIa .
LDL Receptor Disorder .
Apolipoprotein B 100, Familial Defective .
Apolipoprotein B 100, Familial Ligand Defective .
Autosomal Dominant Hypercholesterolemia .
Autosomal Dominant Hypercholesterolemias .
Combined Hyperlipoproteinemia, Familial .
Combined Hyperlipoproteinemias, Familial .
Density Lipoproteinemia, Hyper-Low .
Density Lipoproteinemias, Hyper-Low .
Disorder, LDL Receptor .
Disorders, LDL Receptor .
Dominant Hypercholesterolemia, Autosomal .
Dominant Hypercholesterolemias, Autosomal .
Essential Hypercholesterolemia .
Essential Hypercholesterolemias .
Familial Combined Hyperlipoproteinemias .
Familial Hypercholesterolemia .
Familial Hypercholesterolemias .
Familial Hypercholesterolemic Xanthomatoses .
Familial Hypercholesterolemic Xanthomatosis .
Hyper Low Density Lipoproteinemia .
Hyper beta Lipoproteinemia .
Hyper-Low Density Lipoproteinemias .
Hyper-Low-Density-Lipoproteinemias .
Hyper-beta-Lipoproteinemias .
Hyperbetalipoproteinemias .
Hypercholesterolemias, Autosomal Dominant .
Hypercholesterolemias, Essential .
Hypercholesterolemias, Familial .
Hypercholesterolemic Xanthomatoses, Familial .
Hyperlipoproteinemia Type 2s .
Hyperlipoproteinemia Type IIas .
Hyperlipoproteinemia Type IIbs .
Hyperlipoproteinemia Type IIs .
Hyperlipoproteinemia, Familial Combined .
Hyperlipoproteinemias, Familial Combined .
Hyperlipoproteinemias, Type II .
Hyperlipoproteinemias, Type IIa .
LDL Receptor Disorders .
Lipoproteinemia, Hyper-Low Density .
Lipoproteinemias, Hyper-Low Density .
Receptor Disorder, LDL .
Receptor Disorders, LDL .
Type 2, Hyperlipoproteinemia .
Type II Hyperlipoproteinemia .
Type II Hyperlipoproteinemias .
Type IIa Hyperlipoproteinemia .
Type IIa Hyperlipoproteinemias .
Xanthomatoses, Familial Hypercholesterolemic .
Xanthomatosis, Familial Hypercholesterolemic .
Hypercholesterolemia, Familial .
Hyperbetalipoproteinemia .
Hypercholesterolemia, Essential .
0.54
 
Glycogen Storage Disease Type II .
Acid Alpha-Glucosidase Deficiency .
Acid Maltase Deficiency .
Adult Glycogen Storage Disease Type II .
Alpha-1,4-Glucosidase Deficiency .
Deficiency Disease, Acid Maltase .
Deficiency Disease, Lysosomal alpha-1,4-Glucosidase .
Deficiency of Alpha-Glucosidase .
GAA Deficiency .
GSD II .
GSD2 13663 .
Glycogen Storage Disease II .
Glycogen Storage Disease Type 2 .
Glycogen Storage Disease Type II, Adult .
Glycogen Storage Disease Type II, Infantile .
Glycogen Storage Disease Type II, Juvenile .
Glycogenosis Type II .
Infantile Glycogen Storage Disease Type II .
Juvenile Glycogen Storage Disease Type II .
Pompe's Disease .
Acid Alpha Glucosidase Deficiency .
Acid Alpha-Glucosidase Deficiencies .
Acid Maltase Deficiencies .
Alpha 1,4 Glucosidase Deficiency .
Alpha-1,4-Glucosidase Deficiencies .
Alpha-Glucosidase Deficiencies .
Alpha-Glucosidase Deficiencies, Acid .
Alpha-Glucosidase Deficiency .
Alpha-Glucosidase Deficiency, Acid .
Deficiencies, Acid Alpha-Glucosidase .
Deficiencies, Acid Maltase .
Deficiencies, Alpha-1,4-Glucosidase .
Deficiencies, GAA .
Deficiency of Alpha Glucosidase .
Deficiency, Acid Alpha-Glucosidase .
Deficiency, Acid Maltase .
Deficiency, Alpha-1,4-Glucosidase .
Deficiency, GAA .
Disease, Pompe .
Disease, Pompe's .
GAA Deficiencies .
GSD2s .
Generalized Glycogenoses .
Glycogenoses, Generalized .
Glycogenosis, Generalized .
Lysosomal alpha 1,4 Glucosidase Deficiency Disease .
Maltase Deficiencies, Acid .
Pompes Disease .
Type II, Glycogenosis .
Type IIs, Glycogenosis .
Generalized Glycogenosis .
Glycogenosis 2 .
Pompe Disease .
Acid Maltase Deficiency Disease .
Lysosomal alpha-1,4-Glucosidase Deficiency Disease .
POMPE'S DISEASE .
0.52
 
Dysautonomia, Familial .
Dominant Hereditary Sensory Neuropathy, Type III .
Familial Dysautonomia .
HSAN (Hereditary Sensory and Autonomic Neuropathy) Type III .
HSAN 3 .
HSAN III .
HSAN3 .
HSN-III .
Hereditary Sensory Neuropathy Type 3 .
Hereditary Sensory Neuropathy, Dominant, Type 3 .
Hereditary Sensory Neuropathy, Dominant, Type III .
Hereditary Sensory Neuropathy, Type 3, Dominant .
Hereditary Sensory and Autonomic Neuropathy 3 .
Neuropathy, Hereditary Sensory And Autonomic, Type III .
Type 3 Hereditary Sensory Neuropathy, Dominant .
Type III Hereditary Sensory Neuropathy, Dominant .
Hereditary Sensory and Autonomic Neuropathy Type III .
Riley Day Syndrome .
Riley-Day Syndrome .
HSAN Type III .
Hereditary-Sensory and Autonomic Neuropathy Type III .
Neuropathy, Hereditary and Autonomic, Type III .
0.49
 
Hereditary Sensory and Motor Neuropathy .
CMT4f .
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f .
Charcot-Marie-Tooth Disease, Type 3 .
Dejerine-Sottas Neuropathy .
Dejerine-Sottas Syndrome .
HMSN3 .
Herditary Sensory and Motor Neuropathy .
Hereditary Motor and Sensory Neuropathy .
Hereditary Motor and Sensory Neuropathy 3 .
Hereditary Motor and Sensory Neuropathy Type III .
Hypertrophic Neuropathy of Dejerine-Sottas .
Charcot Marie Tooth Disease, Type 3 .
Dejerine Sottas Disease .
Dejerine Sottas Neuropathy .
Dejerine Sottas Syndrome .
Dejerine-Sottas Hypertrophic Neuropathy .
Disease, Dejerine-Sottas .
HMSN Type IIIs .
HMSN Type VIIs .
Hypertrophic Neuropathy of Dejerine Sottas .
Neuropathy, Dejerine-Sottas .
Syndrome, Dejerine-Sottas .
Type VII, HMSN .
Hereditary Motor and Sensory Neuropathies .
Dejerine-Sottas Disease .
HMSN 13329 .
HMSN Type III .
HMSN Type VII .
Neuropathies, Hereditary Motor and Sensory .
Hereditary, Type III, Motor and Sensory Neuropathy .
Hereditary, Type VII, Motor and Sensory Neuropathy .
HEREDIATARY, TYPE VII, MOTOR AND SENSORY NEUROPATHY .
0.42