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Optic Nerve Optic Disk Optic Chiasm Retinal Ganglion Cells Retina Optic Lobe, Nonmammalian Nerve Fibers Fundus Oculi Mitochondria Chromosomes, Human, Pair 3

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Optic Atrophy Optic Atrophy, Autosomal Dominant Optic Atrophies, Hereditary Atrophy Wolfram Syndrome Optic Atrophy, Hereditary, Leber Muscular Atrophy Optic Neuritis Hereditary Sensory and Motor Neuropathy Papilledema Optic Nerve Injuries Muscular Atrophy, Spinal Vision Disorders Blindness Onchocerciasis, Ocular Eye Diseases Optic Neuropathy, Ischemic Multiple System Atrophy Mitochondrial Diseases Diabetes Insipidus Myoclonic Cerebellar Dyssynergia Vision, Low Syndrome Spinal Muscular Atrophies of Childhood Microcephaly Cerebellar Ataxia Color Vision Defects Optic Nerve Glioma Optic Nerve Diseases Olivopontocerebellar Atrophies Leigh Disease Gyrate Atrophy Deafness Retinal Diseases Hearing Loss, Sensorineural Neurodegenerative Diseases Intellectual Disability Geographic Atrophy Disease Models, Animal Abnormalities, Multiple

Chemicals and Drugs7

GTP Phosphohydrolases DNA, Mitochondrial Glutarates Mitochondrial Proteins Codon, Nonsense NADH Dehydrogenase Membrane Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment8

Pedigree Visual Acuity Electroretinography Magnetic Resonance Imaging DNA Mutational Analysis Visual Field Tests Geographic Mapping Disease Models, Animal

Psychiatry and Psychology4

Visual Acuity Optic Flow Visual Fields Intellectual Disability

Phenomena and Processes16

Visual Acuity Optic Flow Genes, Recessive Mitochondrial Dynamics Mutation Visual Fields Mutation, Missense Evoked Potentials, Visual Codon, Nonsense Consanguinity Genetic Heterogeneity Genes, Dominant Chromosomes, Human, Pair 3 Genetic Linkage Founder Effect Phenotype

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Optics and Photonics

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Maps as Topic Optics and Photonics

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Optic Atrophy Optic Atrophy, Autosomal Dominant Optic Atrophies, Hereditary Atrophy Optic Nerve Wolfram Syndrome Optic Disk GTP Phosphohydrolases Optic Atrophy, Hereditary, Leber Search Engine Muscular Atrophy Optic Neuritis Hereditary Sensory and Motor Neuropathy Optic Chiasm Internet Retinal Ganglion Cells Papilledema Pedigree Optic Nerve Injuries Muscular Atrophy, Spinal Vision Disorders Visual Acuity DNA, Mitochondrial Blindness Onchocerciasis, Ocular Eye Diseases Retina Optic Lobe, Nonmammalian Optic Neuropathy, Ischemic Multiple System Atrophy Glutarates Optic Flow Genes, Recessive Mitochondrial Diseases Diabetes Insipidus Maps as Topic Mitochondrial Dynamics Myoclonic Cerebellar Dyssynergia Vision, Low Mitochondrial Proteins Syndrome Spinal Muscular Atrophies of Childhood Electroretinography Geographic Information Systems Optics and Photonics Mutation Microcephaly Visual Fields Nerve Fibers Cerebellar Ataxia Color Vision Defects Mutation, Missense Optic Nerve Glioma Fundus Oculi Evoked Potentials, Visual Information Storage and Retrieval Mitochondria Blogging Magnetic Resonance Imaging DNA Mutational Analysis Codon, Nonsense Optic Nerve Diseases Olivopontocerebellar Atrophies Software Consanguinity Genetic Heterogeneity NADH Dehydrogenase PubMed Leigh Disease Information Dissemination Visual Field Tests Gyrate Atrophy Deafness Retinal Diseases Genes, Dominant Hearing Loss, Sensorineural Chromosomes, Human, Pair 3 Genetic Linkage Founder Effect Neurodegenerative Diseases Social Media Intellectual Disability Geographic Atrophy Geographic Mapping Disease Models, Animal Phenotype Membrane Proteins Consumer Health Information Abnormalities, Multiple Informatics

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