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Query OMIM entry list
606580
OPA3
OPA3 GENE
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Spinocerebellar Degenerations
Friedreich Ataxia
Spinal Cord Diseases
Spinocerebellar Degenerations
Friedreich Ataxia
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Spinocerebellar Degenerations
Friedreich Ataxia
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Lens Diseases
Cataract
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Spinocerebellar Degenerations
Friedreich Ataxia
Nutritional and Metabolic Diseases
Metabolic Diseases
Mitochondrial Diseases
Friedreich Ataxia
Optic Atrophy, Autosomal Dominant
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
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