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607596
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PONTOCEREBELLAR HYPOPLASIA, TYPE 1
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Multiple System Atrophy
Olivopontocerebellar Atrophies
Cerebellar Diseases
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Movement Disorders
Multiple System Atrophy
Olivopontocerebellar Atrophies
Spinal Cord Diseases
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Multiple System Atrophy
Olivopontocerebellar Atrophies
Olivopontocerebellar Atrophies
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Database Center for Life Science
