Brain optic atrophies hereditary. Medical search. Frequent questions

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Anatomy13

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

Diseases44

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 Brain Injuries Vision Disorders Brain Neoplasms Blindness Onchocerciasis, Ocular Eye Diseases Optic Neuropathy, Ischemic Multiple System Atrophy Mitochondrial Diseases Diabetes Insipidus Syndrome Myoclonic Cerebellar Dyssynergia Vision, Low Spinal Muscular Atrophies of Childhood Microcephaly Cerebellar Ataxia Color Vision Defects Optic Nerve Glioma Disease Models, Animal Optic Nerve Diseases Olivopontocerebellar Atrophies Brain Edema Leigh Disease Neurodegenerative Diseases Deafness Gyrate Atrophy Retinal Diseases Brain Ischemia Hearing Loss, Sensorineural Intellectual Disability Geographic Atrophy 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 Magnetic Resonance Imaging Brain Mapping Electroretinography DNA Mutational Analysis Disease Models, Animal Visual Field Tests

Psychiatry and Psychology4

Visual Acuity Optic Flow Visual Fields Intellectual Disability

Phenomena and Processes17

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

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

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