Loss of vis optic atrophy. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy10

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

Organisms1

Diseases40

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 Spectrophotometry, Ultraviolet Visual Field Tests 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

Disciplines and Occupations1

Optics and Photonics

Technology, Industry, Agriculture2

Optics and Photonics Food Quality

Information Science1

Molecular Sequence Data

Health Care1

Geographicals1

Anatomy Organisms 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 Health Care Geographicals

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 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 Mitochondrial Dynamics Myoclonic Cerebellar Dyssynergia Vision, Low Mitochondrial Proteins Syndrome Spinal Muscular Atrophies of Childhood Electroretinography Optics and Photonics Mutation Microcephaly Visual Fields Nerve Fibers Cerebellar Ataxia Color Vision Defects Mutation, Missense Optic Nerve Glioma Fundus Oculi Evoked Potentials, Visual Mitochondria Magnetic Resonance Imaging DNA Mutational Analysis Spectrophotometry, Ultraviolet Codon, Nonsense Optic Nerve Diseases Olivopontocerebellar Atrophies Citrullus Consanguinity Genetic Heterogeneity NADH Dehydrogenase Croatia Leigh Disease Visual Field Tests Gyrate Atrophy Deafness Food Quality Molecular Sequence Data Retinal Diseases Genes, Dominant Hearing Loss, Sensorineural Chromosomes, Human, Pair 3 Genetic Linkage Founder Effect Neurodegenerative Diseases Intellectual Disability Geographic Atrophy Disease Models, Animal Phenotype Membrane Proteins Abnormalities, Multiple

No FAQ available that match "loss of vis optic atrophy"