Deafness optic atrophy. Medical search. Frequent questions

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Anatomy15

Optic Nerve Optic Disk Optic Chiasm Retinal Ganglion Cells Retina Optic Lobe, Nonmammalian Cochlea Mitochondria Nerve Fibers Fundus Oculi Ear, Inner Hair Cells, Auditory Chromosomes, Human, Pair 3 Stria Vascularis Spiral Ganglion

Diseases43

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

Chemicals and Drugs8

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

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

Psychiatry and Psychology4

Visual Acuity Optic Flow Visual Fields Intellectual Disability

Phenomena and Processes20

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

Disciplines and Occupations1

Optics and Photonics

Technology, Industry, Agriculture1

Optics and Photonics

Information Science2

Molecular Sequence Data Base Sequence

Health Care2

Genetic Testing Family Health

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 Health Care

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

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