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Query OMIM entry list
610708
OPA5
OPTIC ATROPHY 5
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Nervous System Diseases
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
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
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
Nutritional and Metabolic Diseases
Metabolic Diseases
Mitochondrial Diseases
Optic Atrophy, Autosomal Dominant
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