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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 .
C10.228.140.163.100.813 Refsum Disease .
C10.500 Nervous System Malformations .
C10.500.300 Hereditary Sensory and Motor Neuropathy .
C10.500.300.200 Charcot-Marie-Tooth Disease .
C10.500.300.780 Refsum Disease .
C10.500.300.820 Spastic Paraplegia, Hereditary .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.495 Hereditary Sensory and Motor Neuropathy .
C10.574.500.495.200 Charcot-Marie-Tooth Disease .
C10.574.500.495.780 Refsum Disease .
C10.574.500.495.820 Spastic Paraplegia, Hereditary .
C10.668 Neuromuscular Diseases .
C10.668.829 Peripheral Nervous System Diseases .
C10.668.829.800 Polyneuropathies .
C10.668.829.800.300 Hereditary Sensory and Motor Neuropathy .
C10.668.829.800.300.200 Charcot-Marie-Tooth Disease .
C10.668.829.800.300.780 Refsum Disease .
C10.668.829.800.300.820 Spastic Paraplegia, Hereditary .
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 .
C16.131.666.300.780 Refsum Disease .
C16.131.666.300.820 Spastic Paraplegia, Hereditary .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.375 Hereditary Sensory and Motor Neuropathy .
C16.320.400.375.200 Charcot-Marie-Tooth Disease .
C16.320.400.375.780 Refsum Disease .
C16.320.400.375.820 Spastic Paraplegia, Hereditary .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.813 Refsum Disease .
C16.320.565.663 Peroxisomal Disorders .
C16.320.565.663.760 Refsum Disease .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.813 Refsum Disease .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.813 Refsum Disease .
C18.452.648.663 Peroxisomal Disorders .
C18.452.648.663.760 Refsum Disease .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
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 .
1.00
 
Spastic Paraplegia, Hereditary .
Autosomal Dominant Hereditary Spastic Paraplegia .
Autosomal Dominant Spastic Paraplegia Hereditary .
Autosomal Recessive Hereditary Spastic Paraplegia .
Autosomal Recessive Spastic Paraplegia, Hereditary .
CMT with Pyramidal Features .
Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant .
HMSN 5 .
HMSN Type V .
HMSN V .
HMSN V (Hereditary Motor and Sensory Neuropathy Type V) .
Hereditary Autosomal Dominant Spastic Paraplegia .
Hereditary Autosomal Recessive Spastic Paraplegia .
Hereditary Motor And Sensory Neuropathy V .
Hereditary Motor and Sensory Neuropathy 5 .
Hereditary Motor-Sensory Neuropathy with Pyramidal Signs .
Hereditary Spastic Paraplegia, Autosomal Recessive .
Hereditary X-Linked Recessive Spastic Paraplegia .
Hereditary, Spastic Paraplegia, Autosomal Dominant .
Hereditary, Spastic Paraplegia, X-Linked Recessive .
Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia .
Paraplegia, Spastic, Hereditary .
Peroneal Muscular Atrophy with Pyramidal Features, Autosomal Dominant .
Spastic Paraplegia 2 .
Spastic Paraplegia Type 2 .
Spastic Paraplegia, Autosomal Dominant, Hereditary .
Spastic Paraplegia, Autosomal Recessive, Hereditary .
Spastic Paraplegia, Hereditary, Autosomal Dominant .
Spastic Paraplegia, Hereditary, Autosomal Recessive .
Spastic Paraplegia, Hereditary, X-Linked Recessive .
Spastic Paraplegia, X-Linked Recessive, Hereditary .
Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy .
Type V Hereditary Motor and Sensory Neuropathy .
X Linked Recessive Hereditary Spastic Paraplegia .
X-linked Recessive Hereditary Spastic Paraplegia .
Charcot Marie Tooth Disease with Pyramidal Features, Autosomal Dominant .
Hereditary Motor Sensory Neuropathy with Pyramidal Signs .
Hereditary Spastic Paraplegias .
Hereditary X Linked Recessive Spastic Paraplegia .
Hypertrophic Motor Sensory Neuropathy Spastic Paraplegia .
Paraplegia, Hereditary Spastic .
Paraplegias, Hereditary Spastic .
Spastic Paraplegia Hypertrophic Motor Sensory Neuropathy .
Spastic Paraplegias, Hereditary .
Type V, HMSN .
Hereditary Spastic Paraplegia .
X-Linked, Spastic Paraplegia, Hereditary .
PARAPLEGIA, SPASTIC, HEREDITARY .
HMSN TYPE V .
0.86
 
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 .
0.86
 
Refsum Disease .
Adult Refsum Disease .
Classic Refsum Disease .
HMSN 4 .
HMSN IV .
Hemeralopia Heredoataxia Polyneuritiformis .
Hereditary Motor And Sensory Neuropathy IV .
Hereditary Motor and Sensory Neuropathy Type IV .
Hereditary Motor and Sensory Neuropathy, Type IV .
Hereditary Type IV Motor and Sensory Neuropathy .
Phytanic Acid Oxidase Deficiency .
Refsum Disease, Adult .
Refsum Disease, Classic .
Refsum Disease, Phytanic Acid Oxidase Deficiency .
Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency .
Refsum Syndrome .
Refsum's Disease .
Refsum's Syndrome .
Refsum-Thiebaut Syndrome .
Adult Refsum Diseases .
Classic Refsum Diseases .
Disease, Adult Refsum .
Disease, Classic Refsum .
Disease, Refsum .
Disease, Refsum's .
Diseases, Adult Refsum .
Diseases, Classic Refsum .
HMSN IVs .
Heredoataxia Polyneuritiformis, Hemeralopia .
Polyneuritiformis, Hemeralopia Heredoataxia .
Polyneuritiformis, Heredopathia Atactica .
Refsum Disease, Phytanoyl CoA Hydroxylase Deficiency .
Refsum Diseases, Adult .
Refsum Diseases, Classic .
Refsum Thiebaut Syndrome .
Refsum-Thiebaut Syndromes .
Refsums Disease .
Refsums Syndrome .
Syndrome, Refsum .
Syndrome, Refsum's .
Syndrome, Refsum-Thiebaut .
Syndromes, Refsum-Thiebaut .
Heredopathia Atactica Polyneuritiformis .
HMSN Type IV .
Neuropathy, Hereditary Motor and Sensory, Type IV .
Phytanic Acid Storage Disease .
Hereditary-Motor and Sensory-Neuropathy Type IV .
HEREDITARY-MOTOR AND SENSORY NEUROPATHY TYPE IV .
HEREDITARY TYPE IV MOTOR AND SENSORY NEUROPATHY .
NEUROPATHY, HEREDITARY MOTOR AND SENSORY TYPE IV .
REFSUM'S SYNDROME .
REFSUM'S DISEASE .
0.85