Retina specific diseases genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy20

Retina Fundus Oculi Photoreceptor Cells, Vertebrate Photoreceptor Cells Pigment Epithelium of Eye Retinal Cone Photoreceptor Cells Retinal Rod Photoreceptor Cells Retinal Pigment Epithelium Retinal Ganglion Cells Rod Cell Outer Segment Chromosomes, Human, Pair 4 Retinal Vessels Muscle, Skeletal Amacrine Cells X Chromosome Eye Chromosomes, Human, Pair 5 Retinal Bipolar Cells Cornea Choroid

Organisms4

Mice, Inbred mdx Rats, Mutant Strains Mice, Inbred C57BL Mice, Knockout

Diseases48

Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Retinitis Pigmentosa Disease Muscular Dystrophy, Duchenne Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Retinal Diseases Genetic Diseases, Inborn Fuchs' Endothelial Dystrophy Eye Diseases, Hereditary Laurence-Moon Syndrome Communicable Diseases Blindness Genetic Predisposition to Disease Muscular Dystrophy, Facioscapulohumeral Chronic Disease Bardet-Biedl Syndrome Microphthalmos Night Blindness Syndrome Alstrom Syndrome Macular Degeneration Neoplasms Muscular Dystrophy, Emery-Dreifuss Kidney Diseases, Cystic Usher Syndromes Optic Atrophy, Hereditary, Leber Choroid Diseases Neuroaxonal Dystrophies Optic Atrophies, Hereditary Optic Disk Drusen Abnormalities, Multiple Intellectual Disability Disease Models, Animal Muscular Dystrophy, Oculopharyngeal Vision Disorders Reflex Sympathetic Dystrophy Vitelliform Macular Dystrophy Hepatolenticular Degeneration Huntington Disease Neuromuscular Diseases Machado-Joseph Disease Myotonic Disorders Menkes Kinky Hair Syndrome

Chemicals and Drugs23

Eye Proteins cis-trans-Isomerases Peripherins Dystrophin Nerve Tissue Proteins Codon, Nonsense Rhodopsin Genetic Markers Rod Opsins Lipofuscin Sarcoglycans Proteins Carrier Proteins Membrane Proteins Dystroglycans Intermediate Filament Proteins Utrophin ATP-Binding Cassette Transporters Guanylate Cyclase Thymopoietins RNA, Messenger Receptor Protein-Tyrosine Kinases Collagen Type VI

Analytical, Diagnostic and Therapeutic Techniques and Equipment27

Electroretinography Pedigree DNA Mutational Analysis Chromosome Mapping Gene Expression Profiling Visual Acuity Fluorescein Angiography Reproducibility of Results Genetic Testing Risk Factors Tomography, Optical Coherence Retrospective Studies Ophthalmoscopy Cross-Sectional Studies Heteroduplex Analysis Disease Models, Animal Visual Field Tests Polymerase Chain Reaction Sequence Analysis, DNA Models, Genetic Heterozygote Detection Protein Interaction Mapping Fluorescent Antibody Technique, Indirect Amino Acid Substitution Immunohistochemistry Genetic Association Studies Genome-Wide Association Study

Psychiatry and Psychology5

Visual Acuity Visual Fields Intellectual Disability Vision, Ocular Huntington Disease

Phenomena and Processes47

Genes, Recessive Phenotype Consanguinity Mutation Genetic Linkage Genetic Predisposition to Disease Dark Adaptation Genes, Dominant Algorithms Visual Acuity Lod Score Mutation, Missense Exome Exons Haplotypes Codon, Nonsense Homozygote Time Factors Heterozygote Genetic Markers Visual Fields Base Sequence Genotype Frameshift Mutation Polymorphism, Single-Stranded Conformational Light Amino Acid Sequence Vision, Ocular Polymorphism, Single Nucleotide Chromosomes, Human, Pair 4 Genome, Human Trinucleotide Repeat Expansion Alleles Point Mutation Linkage Disequilibrium Genetic Heterogeneity X Chromosome Protein Interaction Maps Gene Regulatory Networks Amino Acid Substitution Fluorescence Genetic Structures Genes Founder Effect Chromosomes, Human, Pair 5 Penetrance Microsatellite Repeats

Disciplines and Occupations4

Computational Biology Genomics Genetics, Medical Immunohistochemistry

Information Science5

Algorithms Molecular Sequence Data Base Sequence Amino Acid Sequence Databases, Genetic

Health Care9

Reproducibility of Results Age Factors Genetic Testing Sex Factors Risk Factors Age of Onset Retrospective Studies Cross-Sectional Studies Genome-Wide Association Study

Geographicals1

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Information Science Health Care Geographicals

Retinal Dystrophies Retina Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Retinitis Pigmentosa Disease Muscular Dystrophy, Duchenne Electroretinography Corneal Dystrophies, Hereditary Eye Proteins cis-trans-Isomerases Pedigree Fundus Oculi Muscular Dystrophy, Animal Retinal Diseases Genes, Recessive Phenotype Consanguinity Photoreceptor Cells, Vertebrate Genetic Diseases, Inborn Mutation Fuchs' Endothelial Dystrophy Eye Diseases, Hereditary Laurence-Moon Syndrome Photoreceptor Cells Communicable Diseases DNA Mutational Analysis Pigment Epithelium of Eye Genetic Linkage Peripherins Blindness Chromosome Mapping Genetic Predisposition to Disease Muscular Dystrophy, Facioscapulohumeral Dark Adaptation Genes, Dominant Dystrophin Computational Biology Gene Expression Profiling Retinal Cone Photoreceptor Cells Retinal Rod Photoreceptor Cells Retinal Pigment Epithelium Chronic Disease Genomics Bardet-Biedl Syndrome Microphthalmos Night Blindness Algorithms Visual Acuity Lod Score Fluorescein Angiography Mutation, Missense Syndrome Exome Alstrom Syndrome Macular Degeneration Reproducibility of Results Exons Neoplasms United States Haplotypes Molecular Sequence Data Muscular Dystrophy, Emery-Dreifuss Nerve Tissue Proteins Kidney Diseases, Cystic Age Factors Mice, Inbred mdx Usher Syndromes Optic Atrophy, Hereditary, Leber Codon, Nonsense Rhodopsin Homozygote Time Factors Choroid Diseases Rats, Mutant Strains Heterozygote Genetic Markers Rod Opsins Genetic Testing Sex Factors Lipofuscin Neuroaxonal Dystrophies Visual Fields Base Sequence Optic Atrophies, Hereditary Risk Factors Optic Disk Drusen Sarcoglycans Age of Onset Tomography, Optical Coherence Genotype Retrospective Studies Proteins Ophthalmoscopy Frameshift Mutation Polymorphism, Single-Stranded Conformational Abnormalities, Multiple Cross-Sectional Studies

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