Symptoms mutations genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy15

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 Cell Line X Chromosome Muscles Myoblasts Cornea

Organisms6

Mice, Inbred mdx Rats, Mutant Strains Mice, Inbred C57BL Mice, Knockout Escherichia coli Mice, Transgenic

Diseases41

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 Syndrome Microphthalmos Bardet-Biedl Syndrome Night Blindness Alstrom Syndrome Muscular Dystrophy, Emery-Dreifuss Optic Atrophy, Hereditary, Leber Usher Syndromes Optic Atrophies, Hereditary Macular Degeneration Neuroaxonal Dystrophies Choroid Diseases Kidney Diseases, Cystic Optic Disk Drusen Abnormalities, Multiple Intellectual Disability Muscular Dystrophy, Oculopharyngeal Reflex Sympathetic Dystrophy Vision Disorders Vitelliform Macular Dystrophy Disease Models, Animal Myotonic Disorders Genetic Predisposition to Disease Muscular Diseases Corneal Dystrophy, Juvenile Epithelial of Meesmann Genetic Diseases, X-Linked

Chemicals and Drugs34

cis-trans-Isomerases Eye Proteins Peripherins Dystrophin Codon, Nonsense Sarcoglycans Membrane Proteins Lipofuscin Carrier Proteins Rhodopsin Nerve Tissue Proteins Proteins Dystroglycans Intermediate Filament Proteins ATP-Binding Cassette Transporters Utrophin Rod Opsins DNA Primers Guanylate Cyclase DNA Receptor Protein-Tyrosine Kinases Codon DNA-Binding Proteins Thymopoietins Transcription Factors Mutant Proteins RNA, Messenger Collagen Type VI Nuclear Proteins Muscle Proteins Lamin Type A Cytoskeletal Proteins Collagen Type VIII Genetic Markers

Analytical, Diagnostic and Therapeutic Techniques and Equipment27

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Polymerase Chain Reaction Chromosome Mapping Amino Acid Substitution Fluorescein Angiography Genetic Testing Heteroduplex Analysis Sequence Analysis, DNA Tomography, Optical Coherence Visual Field Tests Disease Models, Animal Ophthalmoscopy Mutagenesis, Site-Directed Heterozygote Detection Models, Molecular Symptom Assessment Severity of Illness Index Cloning, Molecular Models, Genetic Genetic Complementation Test Sequence Alignment Treatment Outcome Questionnaires Transfection

Psychiatry and Psychology5

Visual Acuity Visual Fields Intellectual Disability Vision, Ocular Depression

Phenomena and Processes52

Mutation, Missense Point Mutation Mutation Genes, Recessive Consanguinity Frameshift Mutation Exons Genes, Dominant Phenotype Codon, Nonsense Heterozygote Base Sequence Germ-Line Mutation Polymorphism, Single-Stranded Conformational Homozygote Visual Acuity Dark Adaptation Genotype Genetic Linkage Amino Acid Substitution Amino Acid Sequence Exome Mutation Rate Visual Fields Alleles Lod Score Haplotypes Mutagenesis Sequence Deletion Polymorphism, Single Nucleotide Protein Structure, Tertiary Gene Deletion Founder Effect Sequence Homology, Amino Acid Vision, Ocular Codon Suppression, Genetic Binding Sites Light X Chromosome Time Factors Trinucleotide Repeat Expansion Fluorescence Genetic Predisposition to Disease Protein Binding Polymorphism, Genetic Transfection Introns Microsatellite Repeats Genes, p53 Plasmids Genetic Markers

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Questionnaires

Health Care6

Genetic Testing Age of Onset Family Health Severity of Illness Index Treatment Outcome Questionnaires

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

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