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
|
| | | | | |
| 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
|
| | | | | |
|