Bilateral progressive optic atrophy. Medical search. Frequent questions

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Anatomy10

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

Diseases43

Optic Atrophy Optic Nerve Diseases Optic Atrophy, Autosomal Dominant Glaucoma 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 Eye Diseases Onchocerciasis, Ocular Multiple System Atrophy Optic Neuropathy, Ischemic Mitochondrial Diseases Syndrome Diabetes Insipidus Myoclonic Cerebellar Dyssynergia Vision, Low Spinal Muscular Atrophies of Childhood Cerebellar Ataxia Microcephaly Color Vision Defects Optic Nerve Glioma Olivopontocerebellar Atrophies Disease Models, Animal Supranuclear Palsy, Progressive Leigh Disease Deafness Hearing Loss, Sensorineural Retinal Diseases Gyrate Atrophy Neurodegenerative Diseases Intellectual Disability Abnormalities, Multiple Geographic Atrophy Disease Progression

Chemicals and Drugs7

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment7

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

Psychiatry and Psychology4

Visual Acuity Optic Flow Visual Fields Intellectual Disability

Phenomena and Processes17

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

Disciplines and Occupations1

Optics and Photonics

Technology, Industry, Agriculture1

Optics and Photonics

Information Science1

Molecular Sequence Data

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Technology, Industry, Agriculture Information Science

Optic Atrophy Optic Nerve Diseases Optic Atrophy, Autosomal Dominant Glaucoma Optic Atrophies, Hereditary Atrophy Optic Nerve Wolfram Syndrome Optic Disk GTP Phosphohydrolases Optic Atrophy, Hereditary, Leber Muscular Atrophy Optic Neuritis Hereditary Sensory and Motor Neuropathy Optic Chiasm Retinal Ganglion Cells Pedigree Papilledema Optic Nerve Injuries Muscular Atrophy, Spinal Vision Disorders Visual Acuity DNA, Mitochondrial Blindness Eye Diseases Retina Onchocerciasis, Ocular Multiple System Atrophy Optic Neuropathy, Ischemic Optic Lobe, Nonmammalian Genes, Recessive Glutarates Optic Flow Mitochondrial Diseases Syndrome Mutation Diabetes Insipidus Myoclonic Cerebellar Dyssynergia Mitochondrial Dynamics Vision, Low Mitochondrial Proteins Electroretinography Spinal Muscular Atrophies of Childhood Magnetic Resonance Imaging Cerebellar Ataxia Visual Fields Mutation, Missense Microcephaly Optics and Photonics Nerve Fibers Color Vision Defects Fundus Oculi Mitochondria DNA Mutational Analysis Optic Nerve Glioma Evoked Potentials, Visual Codon, Nonsense Olivopontocerebellar Atrophies Consanguinity Disease Models, Animal Genetic Heterogeneity NADH Dehydrogenase Supranuclear Palsy, Progressive Leigh Disease Deafness Hearing Loss, Sensorineural Visual Field Tests Genes, Dominant Retinal Diseases Gyrate Atrophy Neurodegenerative Diseases Phenotype Genetic Linkage Chromosomes, Human, Pair 3 Intellectual Disability Membrane Proteins Founder Effect Molecular Sequence Data Abnormalities, Multiple Geographic Atrophy Disease Progression Homozygote

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