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Anatomy11

Fundus Oculi Photoreceptor Cells, Vertebrate Retina Pigment Epithelium of Eye Photoreceptor Cells Retinal Pigment Epithelium Retinal Rod Photoreceptor Cells Retinal Cone Photoreceptor Cells Muscle, Skeletal Rod Cell Outer Segment Chromosomes, Human, Pair 4

Organisms3

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

Diseases37

Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Muscular Dystrophy, Duchenne Retinitis Pigmentosa Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Fuchs' Endothelial Dystrophy Retinal Diseases Laurence-Moon Syndrome Eye Diseases, Hereditary Blindness Muscular Dystrophy, Facioscapulohumeral Bardet-Biedl Syndrome Microphthalmos Night Blindness Alstrom Syndrome Syndrome Muscular Dystrophy, Emery-Dreifuss Usher Syndromes Optic Atrophy, Hereditary, Leber Macular Degeneration Choroid Diseases Neuroaxonal Dystrophies Optic Atrophies, Hereditary Optic Disk Drusen Kidney Diseases, Cystic Abnormalities, Multiple Muscular Dystrophy, Oculopharyngeal Reflex Sympathetic Dystrophy Intellectual Disability Vision Disorders Vitelliform Macular Dystrophy Disease Models, Animal Myotonic Disorders

Chemicals and Drugs24

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment19

Electroretinography Pedigree DNA Mutational Analysis Chromosome Mapping Visual Acuity Fluorescein Angiography Sequence Analysis, DNA Heteroduplex Analysis Polymerase Chain Reaction Tomography, Optical Coherence Gene Expression Profiling Visual Field Tests Genetic Testing Ophthalmoscopy Oligonucleotide Array Sequence Analysis Disease Models, Animal Physical Chromosome Mapping Reverse Transcriptase Polymerase Chain Reaction Cloning, Molecular

Psychiatry and Psychology4

Visual Acuity Visual Fields Intellectual Disability Vision, Ocular

Phenomena and Processes37

Consanguinity Genes, Recessive Mutation Phenotype Genes, Dominant Dark Adaptation Visual Acuity Exons Base Sequence Genetic Linkage Mutation, Missense Codon, Nonsense Exome Expressed Sequence Tags Visual Fields Homozygote Lod Score Amino Acid Sequence Haplotypes Gene Library Heterozygote Polymorphism, Single-Stranded Conformational Genotype Frameshift Mutation Sequence Tagged Sites Polymorphism, Single Nucleotide Chromosomes, Human, Pair 4 Vision, Ocular Point Mutation Genetic Markers Light Genome, Human Gene Expression Regulation Fluorescence Trinucleotide Repeat Expansion Open Reading Frames Gene Expression

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care2

Age of Onset Genetic Testing

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

Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Muscular Dystrophy, Duchenne Retinitis Pigmentosa Corneal Dystrophies, Hereditary Electroretinography cis-trans-Isomerases Eye Proteins Muscular Dystrophy, Animal Fundus Oculi Pedigree Consanguinity Genes, Recessive Fuchs' Endothelial Dystrophy Retinal Diseases Laurence-Moon Syndrome Mutation Eye Diseases, Hereditary Photoreceptor Cells, Vertebrate Retina Peripherins Blindness Muscular Dystrophy, Facioscapulohumeral DNA Mutational Analysis Dystrophin Pigment Epithelium of Eye Bardet-Biedl Syndrome Chromosome Mapping Microphthalmos Phenotype Photoreceptor Cells Night Blindness Molecular Sequence Data Genes, Dominant Alstrom Syndrome Dark Adaptation Visual Acuity Retinal Pigment Epithelium Exons Base Sequence Syndrome Muscular Dystrophy, Emery-Dreifuss Fluorescein Angiography Mice, Inbred mdx Retinal Rod Photoreceptor Cells Genetic Linkage Usher Syndromes Optic Atrophy, Hereditary, Leber Macular Degeneration Mutation, Missense Retinal Cone Photoreceptor Cells Choroid Diseases Neuroaxonal Dystrophies Optic Atrophies, Hereditary Codon, Nonsense Optic Disk Drusen Sarcoglycans Exome Kidney Diseases, Cystic Expressed Sequence Tags Lipofuscin Rats, Mutant Strains Sequence Analysis, DNA Visual Fields Homozygote Heteroduplex Analysis Lod Score Amino Acid Sequence Polymerase Chain Reaction Tomography, Optical Coherence Gene Expression Profiling Abnormalities, Multiple Rhodopsin Haplotypes Muscular Dystrophy, Oculopharyngeal Dystroglycans Visual Field Tests Age of Onset Reflex Sympathetic Dystrophy Nerve Tissue Proteins Genetic Testing Intellectual Disability Proteins Gene Library Heterozygote Membrane Proteins DNA, Complementary Vision Disorders Polymorphism, Single-Stranded Conformational Genotype Utrophin Ophthalmoscopy Vitelliform Macular Dystrophy Frameshift Mutation Oligonucleotide Array Sequence Analysis Carrier Proteins Muscle, Skeletal

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