Neuropathy optic atrophy. Medical search. Frequent questions

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Anatomy14

Optic Nerve Optic Disk Optic Chiasm Retinal Ganglion Cells Retina Sural Nerve Nerve Fibers Optic Lobe, Nonmammalian Fundus Oculi Mitochondria Axons Peripheral Nerves Chromosomes, Human, Pair 3 Sciatic Nerve

Diseases55

Optic Atrophy Optic Atrophy, Autosomal Dominant Optic Atrophies, Hereditary Atrophy Diabetic Neuropathies Wolfram Syndrome Optic Atrophy, Hereditary, Leber Hereditary Sensory and Motor Neuropathy Peripheral Nervous System Diseases Muscular Atrophy Optic Neuritis Optic Neuropathy, Ischemic Papilledema Optic Nerve Injuries Vision Disorders Muscular Atrophy, Spinal Hereditary Sensory and Autonomic Neuropathies Blindness Optic Nerve Diseases Eye Diseases Polyneuropathies Onchocerciasis, Ocular Multiple System Atrophy Mitochondrial Diseases Syndrome Charcot-Marie-Tooth Disease Cerebellar Ataxia Vision, Low Ulnar Neuropathies Diabetes Insipidus Myoclonic Cerebellar Dyssynergia Spinal Muscular Atrophies of Childhood Autonomic Nervous System Diseases Color Vision Defects Microcephaly Optic Nerve Glioma Alcoholic Neuropathy Olivopontocerebellar Atrophies Disease Models, Animal Leigh Disease Hearing Loss, Sensorineural Deafness Retinal Diseases Femoral Neuropathy Gyrate Atrophy Median Neuropathy Neurodegenerative Diseases Glaucoma Amyloid Neuropathies Intellectual Disability Geographic Atrophy Optic Disk Drusen Demyelinating Diseases Cranial Nerve Diseases Abnormalities, Multiple

Chemicals and Drugs7

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment8

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

Psychiatry and Psychology4

Visual Acuity Optic Flow Visual Fields Intellectual Disability

Phenomena and Processes18

Visual Acuity Neural Conduction Genes, Recessive Optic Flow Mutation Visual Fields Mitochondrial Dynamics Mutation, Missense Evoked Potentials, Visual Codon, Nonsense Consanguinity Genetic Heterogeneity Genes, Dominant Phenotype Genetic Linkage Founder Effect Chromosomes, Human, Pair 3 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 Atrophy, Autosomal Dominant Optic Atrophies, Hereditary Atrophy Optic Nerve Diabetic Neuropathies Wolfram Syndrome Optic Atrophy, Hereditary, Leber Optic Disk Hereditary Sensory and Motor Neuropathy GTP Phosphohydrolases Peripheral Nervous System Diseases Muscular Atrophy Optic Neuritis Optic Neuropathy, Ischemic Optic Chiasm Retinal Ganglion Cells Pedigree Papilledema Optic Nerve Injuries Vision Disorders Muscular Atrophy, Spinal Visual Acuity DNA, Mitochondrial Hereditary Sensory and Autonomic Neuropathies Blindness Optic Nerve Diseases Eye Diseases Retina Polyneuropathies Sural Nerve Onchocerciasis, Ocular Nerve Fibers Neural Conduction Genes, Recessive Optic Lobe, Nonmammalian Multiple System Atrophy Mitochondrial Diseases Glutarates Optic Flow Syndrome Mutation Charcot-Marie-Tooth Disease Visual Fields Cerebellar Ataxia Vision, Low Mitochondrial Proteins Ulnar Neuropathies Diabetes Insipidus Mitochondrial Dynamics Myoclonic Cerebellar Dyssynergia Electroretinography Mutation, Missense Spinal Muscular Atrophies of Childhood Fundus Oculi DNA Mutational Analysis Autonomic Nervous System Diseases Evoked Potentials, Visual Magnetic Resonance Imaging Color Vision Defects Mitochondria Optics and Photonics Microcephaly Optic Nerve Glioma NADH Dehydrogenase Alcoholic Neuropathy Codon, Nonsense Consanguinity Axons Visual Field Tests Genetic Heterogeneity Olivopontocerebellar Atrophies Disease Models, Animal Leigh Disease Hearing Loss, Sensorineural Deafness Genes, Dominant Retinal Diseases Femoral Neuropathy Peripheral Nerves Phenotype Gyrate Atrophy Genetic Linkage Median Neuropathy Founder Effect Neurodegenerative Diseases Chromosomes, Human, Pair 3 Glaucoma Amyloid Neuropathies Intellectual Disability Membrane Proteins Sciatic Nerve Tomography, Optical Coherence Geographic Atrophy Optic Disk Drusen Demyelinating Diseases Molecular Sequence Data Homozygote Cranial Nerve Diseases Abnormalities, Multiple

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