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606439
SPG3A
SPG3A GENE
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Damage, Chronic
Cerebral Palsy
Headache Disorders
Headache Disorders, Primary
Migraine Disorders
Migraine without Aura
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
Gait Disorders, Neurologic
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
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Nerve Degeneration
Wallerian Degeneration
Signs and Symptoms
Neurologic Manifestations
Gait Disorders, Neurologic
Paralysis
Paraplegia
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