Optic atrophy autosomal dominant. 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 Chromosomes, Human, Pair 3 Nerve Fibers Chromosomes, Human, Pair 2 Brain

Diseases51

Optic Atrophy Optic Atrophy, Autosomal Dominant Optic Atrophies, Hereditary Atrophy Wolfram Syndrome Polycystic Kidney, Autosomal Dominant Optic Atrophy, Hereditary, Leber Muscular Atrophy Optic Neuritis Hereditary Sensory and Motor Neuropathy Papilledema Syndrome Optic Nerve Injuries Muscular Atrophy, Spinal Vision Disorders Cerebellar Ataxia Blindness Eye Diseases Retinitis Pigmentosa Cataract Onchocerciasis, Ocular Diabetes Insipidus Optic Neuropathy, Ischemic Multiple System Atrophy Hearing Loss, Sensorineural Mitochondrial Diseases Abnormalities, Multiple Color Vision Defects Deafness Myoclonic Cerebellar Dyssynergia Vision, Low Microcephaly Spinal Muscular Atrophies of Childhood Optic Nerve Glioma Disease Models, Animal Olivopontocerebellar Atrophies Spinocerebellar Degenerations Polycystic Kidney Diseases CADASIL Retinal Diseases Optic Nerve Diseases Intellectual Disability Leigh Disease Gyrate Atrophy Neurodegenerative Diseases Dementia, Multi-Infarct Spastic Paraplegia, Hereditary Geographic Atrophy Coloboma Hand Deformities, Congenital Spinocerebellar Ataxias

Chemicals and Drugs10

GTP Phosphohydrolases TRPP Cation Channels DNA, Mitochondrial Codon, Nonsense Glutarates Mitochondrial Proteins Membrane Proteins NADH Dehydrogenase Eye Proteins Genetic Markers

Analytical, Diagnostic and Therapeutic Techniques and Equipment11

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

Psychiatry and Psychology5

Visual Acuity Optic Flow Visual Fields Intellectual Disability Dementia, Multi-Infarct

Phenomena and Processes30

Genes, Dominant Mutation Genetic Linkage Mutation, Missense Genes, Recessive Visual Acuity Phenotype Lod Score Genetic Heterogeneity Codon, Nonsense Optic Flow Haplotypes Visual Fields Mitochondrial Dynamics Base Sequence Consanguinity Chromosomes, Human, Pair 3 Genotype Evoked Potentials, Visual Founder Effect Point Mutation Homozygote Heterozygote Penetrance Genetic Markers Exons Amino Acid Sequence Chromosomes, Human, Pair 2 Frameshift Mutation Gene Deletion

Disciplines and Occupations1

Optics and Photonics

Technology, Industry, Agriculture1

Optics and Photonics

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Family Health Genetic Testing Age of Onset

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 Atrophy Optic Nerve Genes, Dominant Wolfram Syndrome Pedigree GTP Phosphohydrolases Optic Disk Polycystic Kidney, Autosomal Dominant Optic Atrophy, Hereditary, Leber Muscular Atrophy Optic Neuritis Hereditary Sensory and Motor Neuropathy Mutation Optic Chiasm Genetic Linkage Retinal Ganglion Cells DNA Mutational Analysis Mutation, Missense Papilledema Syndrome Genes, Recessive Optic Nerve Injuries Muscular Atrophy, Spinal Visual Acuity Vision Disorders Cerebellar Ataxia Phenotype Lod Score TRPP Cation Channels DNA, Mitochondrial Retina Blindness Eye Diseases Retinitis Pigmentosa Electroretinography Genetic Heterogeneity Chromosome Mapping Cataract Onchocerciasis, Ocular Molecular Sequence Data Codon, Nonsense Diabetes Insipidus Optic Lobe, Nonmammalian Optic Neuropathy, Ischemic Multiple System Atrophy Glutarates Optic Flow Fundus Oculi Hearing Loss, Sensorineural Haplotypes Mitochondrial Diseases Abnormalities, Multiple Mitochondrial Proteins Visual Fields Family Health Magnetic Resonance Imaging Color Vision Defects Deafness Mitochondrial Dynamics Myoclonic Cerebellar Dyssynergia Vision, Low Base Sequence Microcephaly Consanguinity Spinal Muscular Atrophies of Childhood Optics and Photonics Optic Nerve Glioma Mitochondria Chromosomes, Human, Pair 3 Nerve Fibers Genotype Membrane Proteins Evoked Potentials, Visual Disease Models, Animal Founder Effect Olivopontocerebellar Atrophies Point Mutation Spinocerebellar Degenerations Polycystic Kidney Diseases CADASIL Homozygote Retinal Diseases Genetic Testing Heterozygote Visual Field Tests Optic Nerve Diseases Penetrance NADH Dehydrogenase Age of Onset Polymerase Chain Reaction Eye Proteins Intellectual Disability Leigh Disease Genetic Markers Gyrate Atrophy Exons Amino Acid Sequence

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