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230600	-	GM1-GANGLIOSIDOSIS, TYPE II

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Nervous System Diseases

Central Nervous System Diseases

Brain Diseases, Metabolic

Brain Diseases, Metabolic, Inborn

Lysosomal Storage Diseases, Nervous System

Sphingolipidoses

Gangliosidosis, GM1

Cerebellar Diseases

Cerebellar Ataxia

Neurologic Manifestations

Cerebellar Ataxia

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Genetic Diseases, Inborn

Metabolism, Inborn Errors

Brain Diseases, Metabolic, Inborn

Lysosomal Storage Diseases, Nervous System

Sphingolipidoses

Gangliosidosis, GM1

Lipid Metabolism, Inborn Errors

Sphingolipidoses

Gangliosidosis, GM1

Lysosomal Storage Diseases

Lysosomal Storage Diseases, Nervous System

Sphingolipidoses

Gangliosidosis, GM1

Animal Diseases

Pathological Conditions, Signs and Symptoms

Pathologic Processes

Disease Attributes

Chronic Disease

Signs and Symptoms

Neurologic Manifestations

Cerebellar Ataxia

Database Center for Life Science