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258300
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OLIVOPONTOCEREBELLAR ATROPHY II, AUTOSOMAL RECESSIVE
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Digestive System Diseases
Gastrointestinal Diseases
Intestinal Diseases
Malabsorption Syndromes
Celiac Disease
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Cerebellar Ataxia
Movement Disorders
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Eye Diseases
Eye Diseases, Hereditary
Albinism
Lens Diseases
Cataract
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Albinism
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Skin Diseases, Genetic
Albinism
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Skin Diseases, Genetic
Albinism
Nutritional and Metabolic Diseases
Metabolic Diseases
Malabsorption Syndromes
Celiac Disease
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
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