Absent optic atrophy hereditary leber. Medical search. Frequent questions

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Anatomy12

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

Diseases45

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 Papilledema Vision Disorders Optic Nerve Injuries Muscular Atrophy, Spinal Onchocerciasis, Ocular Eye Diseases Mitochondrial Diseases Retinal Degeneration Optic Neuropathy, Ischemic Multiple System Atrophy Diabetes Insipidus Myoclonic Cerebellar Dyssynergia Vision, Low Syndrome Spinal Muscular Atrophies of Childhood Microcephaly Retinal Diseases Cerebellar Ataxia Color Vision Defects Optic Nerve Glioma Retinitis Pigmentosa Retinal Dystrophies Optic Nerve Diseases Disease Models, Animal Olivopontocerebellar Atrophies Leigh Disease Gyrate Atrophy Deafness Eye Diseases, Hereditary Hearing Loss, Sensorineural Neurodegenerative Diseases Intellectual Disability Geographic Atrophy Abnormalities, Multiple

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 Equipment9

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

Psychiatry and Psychology5

Visual Acuity Optic Flow Visual Fields Night Vision Intellectual Disability

Phenomena and Processes21

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

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

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