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Autosomal Recessive Spastic Paraplegia 32
also known as SPG32
Also Known As:
Spastic Paraplegia 32, Autosomal Recessive
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Disease Context: Research Results
Nervous System Diseases: 14178
Neurodegenerative Diseases: 42472
Nervous System Heredodegenerative Disorders: 63
Hereditary Sensory and Motor Neuropathy: 249
Hereditary Spastic Paraplegia: 528
Autosomal Recessive Spastic Paraplegia 32
Neurologic Manifestations: 7102
Neurobehavioral Manifestations: 1586
Intellectual Disability: 8035
Autosomal Recessive Spastic Paraplegia 32
Neuromuscular Diseases: 2005
Peripheral Nervous System Diseases: 11383
Polyneuropathies: 5118
Hereditary Sensory and Motor Neuropathy: 249
Hereditary Spastic Paraplegia: 528
Autosomal Recessive Spastic Paraplegia 32
Nervous System Malformations: 35
Hereditary Sensory and Motor Neuropathy: 249
Hereditary Spastic Paraplegia: 528
Autosomal Recessive Spastic Paraplegia 32
Signs and Symptoms Pathological Conditions
Signs and Symptoms
Neurologic Manifestations: 7102
Neurobehavioral Manifestations: 1586
Intellectual Disability: 8035
Autosomal Recessive Spastic Paraplegia 32
Behavior and Behavior Mechanisms
Neurobehavioral Manifestations: 1586
Intellectual Disability: 8035
Autosomal Recessive Spastic Paraplegia 32
Mental Disorders: 24177
Neurodevelopmental Disorders: 3095
Intellectual Disability: 8035
Autosomal Recessive Spastic Paraplegia 32
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Congenital Abnormalities: 25723
Nervous System Malformations: 35
Hereditary Sensory and Motor Neuropathy: 249
Hereditary Spastic Paraplegia: 528
Autosomal Recessive Spastic Paraplegia 32
Inborn Genetic Diseases: 11939
Nervous System Heredodegenerative Disorders: 63
Hereditary Sensory and Motor Neuropathy: 249
Hereditary Spastic Paraplegia: 528
Autosomal Recessive Spastic Paraplegia 32