Lhon optic atrophy. Medical search. Frequent questions

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Anatomy10

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

Diseases40

Optic Atrophy Optic Atrophy, Autosomal Dominant Optic Atrophies, Hereditary Optic Atrophy, Hereditary, Leber Atrophy Wolfram Syndrome Muscular Atrophy Optic Neuritis Hereditary Sensory and Motor Neuropathy Papilledema Blindness Vision Disorders Optic Nerve Injuries Muscular Atrophy, Spinal Onchocerciasis, Ocular Eye Diseases Optic Neuropathy, Ischemic Multiple System Atrophy Color Vision Defects Optic Nerve Diseases Mitochondrial Diseases Diabetes Insipidus Myoclonic Cerebellar Dyssynergia Vision, Low Syndrome Spinal Muscular Atrophies of Childhood Microcephaly Cerebellar Ataxia Optic Nerve Glioma 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 NADH Dehydrogenase Glutarates Mitochondrial Proteins Codon, Nonsense Membrane Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment8

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

Psychiatry and Psychology4

Visual Acuity Optic Flow Visual Fields Intellectual Disability

Phenomena and Processes19

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

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

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