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 Categorias DeCS

C10 Nervous System Diseases .
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 .
C10.228.140.163.100.362 Hereditary Central Nervous System Demyelinating Diseases .
C10.228.140.163.100.362.375 Canavan Disease .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.228.140.163.100.435.825 Sphingolipidoses .
C10.228.140.163.100.435.825.400 Gaucher Disease .
C10.228.140.695 Leukoencephalopathies .
C10.228.140.695.625 Hereditary Central Nervous System Demyelinating Diseases .
C10.228.140.695.625.375 Canavan Disease .
C10.228.854 Spinal Cord Diseases .
C10.228.854.468 Muscular Atrophy, Spinal .
C10.228.854.468.800 Spinal Muscular Atrophies of Childhood .
C10.314 Demyelinating Diseases .
C10.314.400 Hereditary Central Nervous System Demyelinating Diseases .
C10.314.400.375 Canavan Disease .
C10.500 Nervous System Malformations .
C10.500.300 Hereditary Sensory and Motor Neuropathy .
C10.500.300.200 Charcot-Marie-Tooth Disease .
C10.500.310 Hereditary Sensory and Autonomic Neuropathies .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.300 Canavan Disease .
C10.574.500.495 Hereditary Sensory and Motor Neuropathy .
C10.574.500.495.200 Charcot-Marie-Tooth Disease .
C10.574.500.496 Hereditary Sensory and Autonomic Neuropathies .
C10.574.500.812 Spinal Muscular Atrophies of Childhood .
C10.574.562 Motor Neuron Disease .
C10.574.562.500 Muscular Atrophy, Spinal .
C10.574.562.500.750 Spinal Muscular Atrophies of Childhood .
C10.668 Neuromuscular Diseases .
C10.668.467 Motor Neuron Disease .
C10.668.467.500 Muscular Atrophy, Spinal .
C10.668.467.500.750 Spinal Muscular Atrophies of Childhood .
C10.668.829 Peripheral Nervous System Diseases .
C10.668.829.800 Polyneuropathies .
C10.668.829.800.175 Hereditary Sensory and Autonomic Neuropathies .
C10.668.829.800.300 Hereditary Sensory and Motor Neuropathy .
C10.668.829.800.300.200 Charcot-Marie-Tooth Disease .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.666 Nervous System Malformations .
C16.131.666.300 Hereditary Sensory and Motor Neuropathy .
C16.131.666.300.200 Charcot-Marie-Tooth Disease .
C16.131.666.310 Hereditary Sensory and Autonomic Neuropathies .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.150 Canavan Disease .
C16.320.400.375 Hereditary Sensory and Motor Neuropathy .
C16.320.400.375.200 Charcot-Marie-Tooth Disease .
C16.320.400.415 Hereditary Sensory and Autonomic Neuropathies .
C16.320.400.765 Spinal Muscular Atrophies of Childhood .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C16.320.565.189.362.375 Canavan Disease .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.189.435.825 Sphingolipidoses .
C16.320.565.189.435.825.400 Gaucher Disease .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.803 Sphingolipidoses .
C16.320.565.398.641.803.441 Gaucher Disease .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.825 Sphingolipidoses .
C16.320.565.595.554.825.400 Gaucher Disease .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.132.100.362.375 Canavan Disease .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.132.100.435.825 Sphingolipidoses .
C18.452.132.100.435.825.400 Gaucher Disease .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.441 Gaucher Disease .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.648.189.362.375 Canavan Disease .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.825 Sphingolipidoses .
C18.452.648.189.435.825.400 Gaucher Disease .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.803 Sphingolipidoses .
C18.452.648.398.641.803.441 Gaucher Disease .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.825 Sphingolipidoses .
C18.452.648.595.554.825.400 Gaucher Disease .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.215 Cystatins .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Charcot-Marie-Tooth Disease .
Charcot-Marie Disease .
Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1A .
Charcot-Marie-Tooth Disease, Autosomal Dominant, with Focally Folded Myelin Sheaths, Type 1B .
Charcot-Marie-Tooth Disease, Demyelinating, Type 1A .
Charcot-Marie-Tooth Disease, Demyelinating, Type 1B .
Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy .
Charcot-Marie-Tooth Disease, Type 1A .
Charcot-Marie-Tooth Disease, Type 1B .
Charcot-Marie-Tooth Disease, Type I .
Charcot-Marie-Tooth Disease, Type IA .
Charcot-Marie-Tooth Disease, Type IB .
Charcot-Marie-Tooth Disease, Type II .
Charcot-Marie-Tooth Hereditary Neuropathy .
Charcot-Marie-Tooth Neuropathy, Type 1A .
Charcot-Marie-Tooth Neuropathy, Type 1B .
Charcot-Marie-Tooth Syndrome .
HMN Distal Type I .
HMSN 1A .
HMSN 1B .
HMSN I .
HMSN IA .
HMSN IB .
HMSN II .
HMSN1A .
HMSN1B .
Hereditary Areflexic Dystasia .
Hereditary Motor And Sensory Neuropathy IB .
Hereditary Motor and Sensory Neuropathy 1A .
Hereditary Motor and Sensory Neuropathy 1B .
Hereditary Motor and Sensory Neuropathy IA .
Hereditary Type I Motor and Sensory Neuropathy .
Neuropathy, Type I Hereditary Motor and Sensory .
Neuropathy, Type II Hereditary Motor and Sensory .
Roussy Levy Hereditary Areflexic Dystasia .
Roussy-Levy Disease .
Roussy-Levy Hereditary Areflexic Dystasia .
Areflexic Dystasia, Hereditary .
Areflexic Dystasias, Hereditary .
Atrophies, Peroneal Muscular .
Atrophy, Peroneal Muscular .
Charcot Marie Disease .
Charcot Marie Tooth Disease .
Charcot Marie Tooth Disease, Type 1A .
Charcot Marie Tooth Disease, Type 1B .
Charcot Marie Tooth Disease, Type I .
Charcot Marie Tooth Disease, Type IA .
Charcot Marie Tooth Disease, Type IB .
Charcot Marie Tooth Disease, Type II .
Charcot Marie Tooth Hereditary Neuropathy .
Charcot Marie Tooth Neuropathy, Type 1A .
Charcot Marie Tooth Neuropathy, Type 1B .
Charcot Marie Tooth Syndrome .
Dystasia, Hereditary Areflexic .
Dystasias, Hereditary Areflexic .
Hereditary Areflexic Dystasias .
Hereditary Motor and Sensory Neuropathy Type II .
Hereditary Neuropathy, Charcot-Marie-Tooth .
Muscular Atrophies, Peroneal .
Peroneal Muscular Atrophies .
Roussy Levy Disease .
Roussy Levy Syndrome .
Syndrome, Charcot-Marie-Tooth .
Syndrome, Roussy-Levy .
Atrophy, Muscular, Peroneal .
Muscular Atrophy, Peroneal .
Peroneal Muscular Atrophy .
Hereditary Motor, and Sensory Neuropathy Type I .
Hereditary Motor and Sensory-Neuropathy Type II .
HMSN Type I .
HMSN Type II .
Roussy-Levy Syndrome .
HERDITARY MOTOR, AND SENSORY NEUROPATHY TYPE I .
HMN DISTAL TYPE I .
HEREDITARY TYPE I MOTOR AND SENSORY NEUROPATHY .
NEUROPATHY, TYPE I HEREDITARY MOTOR AND SENSORY .
CHARCOT-MARIE DISEASE .
1.00
 
Spinal Muscular Atrophies of Childhood .
HMN (Hereditary Motor Neuropathy) Proximal Type I .
Kugelberg-Welander Syndrome .
Muscular Atrophy, Infantile .
Muscular Atrophy, Juvenile .
Muscular Atrophy, Spinal, Infantile Chronic Form .
Muscular Atrophy, Spinal, Intermediate Type .
Muscular Atrophy, Spinal, Type I .
Muscular Atrophy, Spinal, Type II .
Muscular Atrophy, Spinal, Type III .
Proximal Hereditary Motor Neuropathy Type I .
SMA, Infantile Acute Form .
Spinal Muscular Atrophy 1 .
Spinal Muscular Atrophy Type 2 .
Spinal Muscular Atrophy Type I .
Spinal Muscular Atrophy Type II .
Spinal Muscular Atrophy Type III .
Spinal Muscular Atrophy, Mild Childhood and Adolescent Form .
Spinal Muscular Atrophy, Type 3 .
Spinal Muscular Atrophy, Type I .
Spinal Muscular Atrophy, Type II .
Spinal Muscular Atrophy, Type III .
Type I Spinal Muscular Atrophy .
Type II Spinal Muscular Atrophy .
Type III Spinal Muscular Atrophy .
Werdnig Hoffman Disease .
Infantile Muscular Atrophy .
Juvenile Muscular Atrophy .
Kugelberg Welander Disease .
Kugelberg Welander Syndrome .
Werdnig Hoffmann Disease .
Infantile Spinal Muscular Atrophy .
Muscular Atrophy, Spinal, Infantile .
Spinal Muscular Atrophy, Infantile .
Werdnig-Hoffmann Disease .
Juvenile Spinal Muscular Atrophy .
Kugelberg-Welander Disease .
Spinal Muscular Atrophy, Juvenile .
HMN Proximal Type I .
KUGLEBERG-WELANDER DISEASE .
0.69
 
Canavan Disease .
ACY2 Deficiency .
ASP Deficiency .
ASPA Deficiency .
Aminoacylase 2 Deficiency .
Aspartoacylase Deficiency .
Canavan Disease, Familial Form .
Canavan Disease, Infantile .
Canavan Disease, Juvenile .
Canavan Disease, Neonatal .
Canavan Disease, Sporadic Form .
Canavan Disease, Type I .
Canavan Disease, Type II .
Canavan Disease, Type III .
Canavan-van Bogaert-Bertrand Disease .
Deficiency Disease, Aspartoacylase .
Familial Form of Canavan Disease .
Infantile Canavan Disease .
Juvenile Canavan Disease .
Leukodystrophy, Spongiform .
Neonatal Canavan Disease .
Spongy Degeneration Of Central Nervous System .
Spongy Degeneration of Infancy .
Spongy Degeneration of White Matter In Infancy .
Spongy Degeneration of the Brain .
Spongy Degeneration of the Central Nervous System .
Spongy Disease of Central Nervous System .
Spongy Disease of White Matter .
Sporadic Form of Canavan Disease .
Type I Canavan Disease .
Type II Canavan Disease .
Type III Canavan Disease .
Van Bogaert-Bertrand Syndrome .
Von Bogaert-Bertrand Disease .
Canavan van Bogaert Bertrand Disease .
Disease, Canavan .
Disease, Canavan-van Bogaert-Bertrand .
Disease, Von Bogaert-Bertrand .
Spongiform Leukodystrophy .
Syndrome, Van Bogaert-Bertrand .
Van Bogaert Bertrand Syndrome .
Von Bogaert Bertrand Disease .
Canavan-van Bogaert-Bertrand Disease .
Leukodystrophy, Spongiform .
Spongy Disease of White Matter .
0.53
 
Gaucher Disease .
Acid beta-Glucosidase Deficiency .
Acid beta-Glucosidase Deficiency Disease .
Acute Neuronopathic Gaucher Disease .
Chronic Gaucher Disease .
GBA Deficiency .
Gaucher Disease Type 3 .
Gaucher Disease, Acute Neuronopathic .
Gaucher Disease, Acute Neuronopathic Type .
Gaucher Disease, Chronic .
Gaucher Disease, Chronic Neuronopathic Type .
Gaucher Disease, Infantile .
Gaucher Disease, Infantile Cerebral .
Gaucher Disease, Juvenile .
Gaucher Disease, Juvenile and Adult, Cerebral .
Gaucher Disease, Neuronopathic .
Gaucher Disease, Non-Neuronopathic Form .
Gaucher Disease, Noncerebral Juvenile .
Gaucher Disease, Subacute Neuronopathic Form .
Gaucher Disease, Subacute Neuronopathic Type .
Gaucher Disease, Type 1 .
Gaucher Disease, Type 2 .
Gaucher Disease, Type 3 .
Gaucher Disease, Type I .
Gaucher Disease, Type II .
Gaucher Disease, Type III .
Gaucher Splenomegaly .
Gaucher Syndrome .
Gaucher's Disease .
Gauchers Disease .
Glucocerebrosidase Deficiency .
Glucocerebrosidosis .
Glucosyl Cerebroside Lipidosis .
Glucosylceramidase Deficiency .
Glucosylceramide Beta-Glucosidase Deficiency .
Glucosylceramide Lipidosis .
Infantile Gaucher Disease .
Kerasin Histiocytosis .
Kerasin Lipoidosis .
Kerasin thesaurismosis .
Lipoid Histiocytosis (Kerasin Type) .
Non-Neuronopathic Gaucher Disease .
Subacute Neuronopathic Gaucher Disease .
Type 1 Gaucher Disease .
Type 2 Gaucher Disease .
Type 3 Gaucher Disease .
Cerebroside Lipidoses, Glucosyl .
Cerebroside Lipidosis Syndromes .
Cerebroside Lipidosis, Glucosyl .
Deficiencies, GBA .
Deficiencies, Glucocerebrosidase .
Deficiency Disease, Glucocerebrosidase .
Deficiency Diseases, Glucocerebrosidase .
Deficiency, GBA .
Deficiency, Glucocerebrosidase .
Disease, Chronic Gaucher .
Disease, Gaucher .
Disease, Gaucher's .
Disease, Gauchers .
Disease, Glucocerebrosidase Deficiency .
Disease, Infantile Gaucher .
Disease, Juvenile Gaucher .
Disease, Neuronopathic Gaucher .
Disease, Non-Neuronopathic Gaucher .
Diseases, Gauchers .
Diseases, Glucocerebrosidase Deficiency .
GBA Deficiencies .
Gaucher Disease, Non Neuronopathic Form .
Gaucher Disease, Non-Neuronopathic .
Gauchers Diseases .
Glucocerebrosidase Deficiencies .
Glucocerebrosidase Deficiency Diseases .
Glucocerebrosidoses .
Glucosyl Cerebroside Lipidoses .
Glucosylceramide Lipidoses .
Histiocytoses, Kerasin .
Histiocytoses, Lipoid (Kerasin Type) .
Histiocytosis, Kerasin .
Histiocytosis, Lipoid (Kerasin Type) .
Juvenile Gaucher Disease .
Kerasin Histiocytoses .
Kerasin Lipoidoses .
Kerasin thesaurismoses .
Lipidoses, Glucosyl Cerebroside .
Lipidoses, Glucosylceramide .
Lipidosis Syndrome, Cerebroside .
Lipidosis Syndromes, Cerebroside .
Lipidosis, Glucosyl Cerebroside .
Lipidosis, Glucosylceramide .
Lipoid Histiocytoses (Kerasin Type) .
Lipoidoses, Kerasin .
Lipoidosis, Kerasin .
Non Neuronopathic Gaucher Disease .
Splenomegaly, Gaucher .
Syndrome, Cerebroside Lipidosis .
Syndrome, Gaucher .
Syndromes, Cerebroside Lipidosis .
thesaurismoses, Kerasin .
thesaurismosis, Kerasin .
Cerebroside Lipidosis Syndrome .
Glucocerebrosidase Deficiency Disease .
Glucosylceramide Beta-Glucosidase Deficiency Disease .
Neuronopathic Gaucher Disease .
Gaucher Disease Type 1 .
Gaucher Disease Type 2 .
GAUCHER'S DISEASE .
0.51
 
Cystatins .
Cystatin-Related Proteins .
Stefins .
Type 1 Cystatins .
Type 2 Cystatins .
Type 3 Cystatins .
Type I Cystatins .
Type II Cystatins .
Type III Cystatins .
Cystatin Related Proteins .
Cystatins, Type 1 .
Cystatins, Type 2 .
Cystatins, Type 3 .
Cystatins, Type I .
Cystatins, Type II .
Cystatins, Type III .
Cystatin Superfamily .
0.47
 
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 .
0.46