Occur dystrophy genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy17

X Chromosome Muscles Fundus Oculi Photoreceptor Cells, Vertebrate Retina Pigment Epithelium of Eye Photoreceptor Cells Retinal Pigment Epithelium Muscle, Skeletal Retinal Cone Photoreceptor Cells Retinal Rod Photoreceptor Cells Myoblasts Cornea Sarcolemma Chromosomes, Human, Pair 4 Muscle Fibers, Skeletal Rod Cell Outer Segment

Organisms2

Mice, Inbred mdx Rats, Mutant Strains

Diseases39

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

Chemicals and Drugs25

Dystrophin cis-trans-Isomerases Eye Proteins Peripherins Sarcoglycans Dystroglycans Utrophin Codon, Nonsense Lipofuscin Thymopoietins Rhodopsin Intermediate Filament Proteins Collagen Type VI Membrane Proteins Nerve Tissue Proteins Collagen Type VIII Carrier Proteins Dystrophin-Associated Proteins Rod Opsins Proteins Creatine Kinase ATP-Binding Cassette Transporters Guanylate Cyclase Muscle Proteins Lamin Type A

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Fluorescein Angiography Chromosome Mapping Tomography, Optical Coherence Heteroduplex Analysis Visual Field Tests Ophthalmoscopy Genetic Testing Disease Models, Animal Polymerase Chain Reaction Heterozygote Detection Keratoplasty, Penetrating

Psychiatry and Psychology3

Visual Acuity Visual Fields Intellectual Disability

Phenomena and Processes26

X Chromosome Consanguinity Genes, Recessive Mutation Visual Acuity Genes, Dominant Phenotype Dark Adaptation Exons Mutation, Missense Codon, Nonsense Genetic Linkage Visual Fields Heterozygote Homozygote Exome Frameshift Mutation Lod Score Base Sequence Polymorphism, Single-Stranded Conformational Haplotypes Trinucleotide Repeat Expansion Genotype Chromosomes, Human, Pair 4 Amino Acid Sequence Point Mutation

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

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