Ocular optic atrophy hereditary leber. Medical search. Frequent questions

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Anatomy14

Optic Nerve Optic Disk Optic Chiasm Retinal Ganglion Cells Retina Eye Fundus Oculi Optic Lobe, Nonmammalian Mitochondria Nerve Fibers Photoreceptor Connecting Cilium Photoreceptor Cells, Vertebrate Chromosomes, Human, Pair 3 Cornea

Diseases54

Optic Atrophy Optic Atrophy, Autosomal Dominant Optic Atrophies, Hereditary Optic Atrophy, Hereditary, Leber Leber Congenital Amaurosis Atrophy Wolfram Syndrome Blindness Muscular Atrophy Optic Neuritis Hereditary Sensory and Motor Neuropathy Vision Disorders Papilledema Optic Nerve Injuries Muscular Atrophy, Spinal Onchocerciasis, Ocular Eye Diseases Mitochondrial Diseases Retinal Degeneration Optic Neuropathy, Ischemic Ocular Hypertension Multiple System Atrophy Retinal Diseases Syndrome Vision, Low Diabetes Insipidus Myoclonic Cerebellar Dyssynergia Spinal Muscular Atrophies of Childhood Microcephaly Cerebellar Ataxia Color Vision Defects Toxoplasmosis, Ocular Optic Nerve Diseases Disease Models, Animal Optic Nerve Glioma Retinitis Pigmentosa Retinal Dystrophies Glaucoma Olivopontocerebellar Atrophies Eye Diseases, Hereditary Leigh Disease Albinism, Ocular Deafness Gyrate Atrophy Cataract Hearing Loss, Sensorineural Eye Neoplasms Abnormalities, Multiple Intellectual Disability Neurodegenerative Diseases Eye Injuries Geographic Atrophy Ocular Motility Disorders Glaucoma, Open-Angle

Chemicals and Drugs9

GTP Phosphohydrolases cis-trans-Isomerases DNA, Mitochondrial Eye Proteins NADH Dehydrogenase Glutarates Codon, Nonsense Mitochondrial Proteins Membrane Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment13

Pedigree Visual Acuity Electroretinography DNA Mutational Analysis Disease Models, Animal Magnetic Resonance Imaging Tomography, Optical Coherence Visual Field Tests Tonometry, Ocular Refraction, Ocular Ophthalmoscopy Genetic Testing Chromosome Mapping

Psychiatry and Psychology6

Visual Acuity Visual Fields Optic Flow Vision, Ocular Night Vision Intellectual Disability

Phenomena and Processes28

Visual Acuity Mutation Genes, Recessive Visual Fields Optic Flow Consanguinity Mutation, Missense Codon, Nonsense Mitochondrial Dynamics Evoked Potentials, Visual Intraocular Pressure Phenotype Vision, Ocular Genetic Linkage Genetic Heterogeneity Homozygote Penetrance Genes, Dominant Refraction, Ocular Chromosomes, Human, Pair 3 Dominance, Ocular Ocular Physiological Phenomena Night Vision Haplotypes Founder Effect Base Sequence Genotype Point Mutation

Disciplines and Occupations1

Optics and Photonics

Technology, Industry, Agriculture1

Optics and Photonics

Information Science2

Molecular Sequence Data Base Sequence

Health Care1

Genetic Testing

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 Optic Atrophies, Hereditary Optic Atrophy, Hereditary, Leber Leber Congenital Amaurosis Atrophy Optic Nerve Wolfram Syndrome Optic Disk GTP Phosphohydrolases Blindness Muscular Atrophy Optic Neuritis cis-trans-Isomerases Pedigree Hereditary Sensory and Motor Neuropathy Optic Chiasm Retinal Ganglion Cells DNA, Mitochondrial Visual Acuity Vision Disorders Papilledema Retina Electroretinography Optic Nerve Injuries Muscular Atrophy, Spinal Mutation Onchocerciasis, Ocular Eye Proteins DNA Mutational Analysis Eye Genes, Recessive Fundus Oculi Eye Diseases Mitochondrial Diseases NADH Dehydrogenase Retinal Degeneration Visual Fields Optic Lobe, Nonmammalian Optic Neuropathy, Ischemic Ocular Hypertension Multiple System Atrophy Glutarates Retinal Diseases Optic Flow Consanguinity Mutation, Missense Syndrome Vision, Low Codon, Nonsense Diabetes Insipidus Mitochondrial Dynamics Myoclonic Cerebellar Dyssynergia Mitochondrial Proteins Optics and Photonics Spinal Muscular Atrophies of Childhood Mitochondria Nerve Fibers Microcephaly Cerebellar Ataxia Color Vision Defects Evoked Potentials, Visual Photoreceptor Connecting Cilium Toxoplasmosis, Ocular Optic Nerve Diseases Disease Models, Animal Optic Nerve Glioma Retinitis Pigmentosa Magnetic Resonance Imaging Tomography, Optical Coherence Intraocular Pressure Phenotype Retinal Dystrophies Vision, Ocular Genetic Linkage Glaucoma Olivopontocerebellar Atrophies Visual Field Tests Genetic Heterogeneity Molecular Sequence Data Eye Diseases, Hereditary Tonometry, Ocular Photoreceptor Cells, Vertebrate Homozygote Membrane Proteins Leigh Disease Albinism, Ocular Deafness Penetrance Gyrate Atrophy Cataract Genes, Dominant Refraction, Ocular Hearing Loss, Sensorineural Chromosomes, Human, Pair 3 Eye Neoplasms Dominance, Ocular Ocular Physiological Phenomena Abnormalities, Multiple Night Vision

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