MeSH Treeview
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600363
SPG6
SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT
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Musculoskeletal Diseases
Muscular Diseases
Muscle Spasticity
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Movement Disorders
Angelman Syndrome
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Prader-Willi Syndrome
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Spasticity
Paralysis
Paraplegia
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Angelman Syndrome
Prader-Willi Syndrome
Chromosome Disorders
Angelman Syndrome
Prader-Willi Syndrome
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Genetic Diseases, Inborn
Chromosome Disorders
Angelman Syndrome
Prader-Willi Syndrome
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Nutritional and Metabolic Diseases
Nutrition Disorders
Overnutrition
Obesity
Prader-Willi Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Spasticity
Paralysis
Paraplegia
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