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 Categorias DeCS

C02 Virus Diseases .
C02.256 DNA Virus Infections .
C02.256.466 Herpesviridae Infections .
C02.256.466.930 Varicella Zoster Virus Infection .
C02.256.466.930.750 Herpes Zoster .
C02.256.466.930.750.733 Herpes Zoster Oticus .
C07 Stomatognathic Diseases .
C07.465 Mouth Diseases .
C07.465.299 Facial Nerve Diseases .
C07.465.299.750 Herpes Zoster Oticus .
C09 Otorhinolaryngologic Diseases .
C09.218 Ear Diseases .
C09.218.513 Herpes Zoster Oticus .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.079 Basal Ganglia Diseases .
C10.228.140.079.862 Parkinsonian Disorders .
C10.228.140.252 Cerebellar Diseases .
C10.228.140.252.700 Spinocerebellar Degenerations .
C10.228.140.252.700.250 Myoclonic Cerebellar Dyssynergia .
C10.228.662 Movement Disorders .
C10.228.662.600 Parkinsonian Disorders .
C10.228.854 Spinal Cord Diseases .
C10.228.854.787 Spinocerebellar Degenerations .
C10.228.854.787.500 Myoclonic Cerebellar Dyssynergia .
C10.292 Cranial Nerve Diseases .
C10.292.319 Facial Nerve Diseases .
C10.292.319.750 Herpes Zoster Oticus .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.825 Spinocerebellar Degenerations .
C10.574.500.825.250 Myoclonic Cerebellar Dyssynergia .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C10.597.606.643.455 Mental Retardation, X-Linked .
C10.597.606.643.455.750 Mucopolysaccharidosis II .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.500 Mental Retardation, X-Linked .
C16.320.322.500.750 Mucopolysaccharidosis II .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.525 Mental Retardation, X-Linked .
C16.320.400.525.750 Mucopolysaccharidosis II .
C16.320.400.780 Spinocerebellar Degenerations .
C16.320.400.780.500 Myoclonic Cerebellar Dyssynergia .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.715 Mucopolysaccharidoses .
C16.320.565.202.715.645 Mucopolysaccharidosis II .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.600 Mucopolysaccharidoses .
C16.320.565.595.600.645 Mucopolysaccharidosis II .
C17 Skin and Connective Tissue Diseases .
C17.300 Connective Tissue Diseases .
C17.300.550 Mucinoses .
C17.300.550.575 Mucopolysaccharidoses .
C17.300.550.575.645 Mucopolysaccharidosis II .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.715 Mucopolysaccharidoses .
C18.452.648.202.715.645 Mucopolysaccharidosis II .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.600 Mucopolysaccharidoses .
C18.452.648.595.600.645 Mucopolysaccharidosis II .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Parkinsonian Disorders .
Autosomal Dominant Juvenile Parkinson Disease .
Autosomal Dominant Juvenile Parkinsonism .
Autosomal Dominant Parkinsonism .
Autosomal Recessive Juvenile Parkinson Disease .
Autosomal Recessive Parkinsonism .
Autosomal Recesssive Juvenile Parkinsonism .
Chromosome 6-Linked Autosomal Recessive Parkinsonism .
Experimental Parkinson Disease .
Experimental Parkinsonism .
Experimental Parkinsonism, MPTP-Induced .
Familial Parkinson Disease, Autosomal Recessive .
Juvenile Parkinson Disease .
Juvenile Parkinson Disease, Autosomal Dominant .
Juvenile Parkinson Disease, Autosomal Recessive .
Juvenile Parkinsonism, Autosomal Dominant .
Juvenile Parkinsonism, Autosomal Recessive .
MPTP-Induced Experimental Parkinsonism .
Parkinson Disease 2 .
Parkinson Disease 2, Autosomal Recessive Juvenile .
Parkinson Disease Autosomal Recessive, Early Onset .
Parkinson Disease, Autosomal Dominant. Juvenile .
Parkinson Disease, Experimental .
Parkinson Disease, Familial, Autosomal Recessive .
Parkinson Disease, Juvenile .
Parkinson Disease, Juvenile, Autosomal Dominant .
Parkinson Disease, Juvenile, Autosomal Recessive .
Parkinsonian Diseases .
Parkinsonian Syndromes .
Parkinsonism, Early Onset, with Diurnal Fluctuation .
Parkinsonism, Early-Onset, With Diurnal Fluctuation .
Parkinsonism, Juvenile, Autosomal Dominant .
Parkinsonism, Juvenile, Autosomal Recessive .
Chromosome 6 Linked Autosomal Recessive Parkinsonism .
Diseases, Experimental Parkinson .
Dominant Parkinsonism, Autosomal .
Experimental Parkinson Diseases .
Experimental Parkinsonism, MPTP Induced .
Experimental Parkinsonisms .
Juvenile Parkinsonism .
Juvenile Parkinsonism, Familial .
Juvenile Parkinsonisms .
MPTP Induced Experimental Parkinsonism .
Parkinson Diseases, Experimental .
Parkinsonism, Autosomal Dominant .
Parkinsonism, Autosomal Recessive .
Parkinsonism, Familial Juvenile .
Parkinsonism, MPTP-Induced Experimental .
Parkinsonisms, Experimental .
Parkinsonisms, Juvenile .
Recessive Parkinsonism, Autosomal .
Familial Juvenile Parkinsonism .
Parkinsonian Syndrome .
Parkinsonism .
Parkinsonism, Experimental .
Parkinsonism, Juvenile .
Ramsay Hunt Paralysis Syndrome .
1.00
 
Herpes Zoster Oticus .
Auricular Syndrome of Ramsay Hunt .
Herpes Zoster Auricularis .
Herpes Zoster Cephalicus .
Herpetic Geniculate Ganglionitis .
Ganglionitis, Herpetic Geniculate .
Geniculate Ganglionitides, Herpetic .
Geniculate Ganglionitis, Herpetic .
Geniculate Neuralgia .
Geniculate Neuralgias .
Herpes Zoster, Geniculate .
Herpetic Geniculate Ganglionitides .
Neuralgias, Geniculate .
Syndrome, Ramsay Hunt .
Neuralgia, Geniculate .
Ramsay Hunt Auricular Syndrome .
Ramsay Hunt Syndrome .
Geniculate Herpes Zoster .
HERPES ZOSTER AURICULARIS .
0.82
 
Myoclonic Cerebellar Dyssynergia .
Cerebelloparenchymal Disorder V .
Dentate Cerebellar Ataxia .
Dentate Nucleus Syndrome, Ramsay Hunt .
Dyssynergia Cerebellaris Myoclonica Of Hunt .
Dyssynergia Cerebellaris Progressiva .
Ramsay Hunt Dentate Syndrome .
Spinodentate Atrophy .
Ataxia, Dentate Cerebellar .
Ataxias, Dentate Cerebellar .
Atrophies, Dentate Cerebellar .
Atrophy, Dentate Cerebellar .
Cerebellar Ataxias, Dentate .
Cerebellar Atrophy, Dentate .
Cerebellar Dyssynergia, Myoclonic .
Cerebellar Dyssynergias .
Cerebellar Dyssynergias, Myoclonic .
Dentate Cerebellar Ataxias .
Dentate Cerebellar Atrophies .
Dyssynergia, Cerebellar .
Dyssynergia, Myoclonic Cerebellar .
Dyssynergias, Cerebellar .
Dyssynergias, Myoclonic Cerebellar .
Myoclonic Cerebellar Dyssynergias .
Ramsay Hunt Cerebellar Syndrome .
Cerebellar Dyssynergia .
Dentate Cerebellar Atrophy .
Dyssynergia Cerebellaris Myoclonica .
RAMSAY HUNT DENTATE SYNDROME .
0.72
 
Mucopolysaccharidosis II .
Hunter Syndrome .
Hunter Syndrome Gargoylism .
I2S Deficiency .
Mucopolysaccharidosis 2 .
Mucopolysaccharidosis Type 2 .
Mucopolysaccharidosis Type II .
Deficiency, I2S .
Deficiency, Iduronate 2-Sulfatase .
Deficiency, Iduronate Sulfatase .
Deficiency, Sulfoiduronate Sulfatase .
Hunters Syndrome .
Iduronate 2 Sulfatase Deficiency .
Syndrome, Hunter .
Syndrome, Hunter's .
Gargoylism, Hunter Syndrome .
Hunter's Syndrome .
Iduronate 2-Sulfatase Deficiency .
Iduronate Sulfatase Deficiency .
Sulfoiduronate Sulfatase Deficiency .
0.57