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165500
OPA1
OPTIC ATROPHY 1
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Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Demyelinating Diseases
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Paralysis
Ophthalmoplegia
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Vision Disorders
Blindness
Color Vision Defects
Scotoma
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Eyelid Diseases
Blepharoptosis
Lens Diseases
Cataract
Ocular Hypertension
Glaucoma
Glaucoma, Open-Angle
Ocular Motility Disorders
Ophthalmoplegia
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Retinal Diseases
Retinal Neovascularization
Vision Disorders
Blindness
Color Vision Defects
Scotoma
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Diseases
Optic Atrophy, Autosomal Dominant
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Metaplasia
Neovascularization, Pathologic
Retinal Neovascularization
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Paralysis
Ophthalmoplegia
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Vision Disorders
Blindness
Color Vision Defects
Scotoma
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