Dystrophy phenotype retinal dystrophies. Medical search. Frequent questions

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Anatomy22

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 Muscles Cornea Chromosomes, Human, Pair 4 Muscle Fibers, Skeletal Sarcolemma Rod Cell Outer Segment X Chromosome Descemet Membrane Cells, Cultured Endothelium, Corneal Cell Line Corneal Stroma

Organisms5

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

Diseases50

Retinal Dystrophies Muscular Dystrophies Muscular Dystrophy, Emery-Dreifuss 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 Laurence-Moon Syndrome Eye Diseases, Hereditary Neuroaxonal Dystrophies Blindness Night Blindness Bardet-Biedl Syndrome Microphthalmos Muscular Dystrophy, Oculopharyngeal Reflex Sympathetic Dystrophy Syndrome Vitelliform Macular Dystrophy Alstrom Syndrome Macular Degeneration Choroid Diseases Usher Syndromes Optic Atrophy, Hereditary, Leber Optic Atrophies, Hereditary Kidney Diseases, Cystic Optic Disk Drusen Disease Models, Animal Abnormalities, Multiple Myotonic Disorders Intellectual Disability Vision Disorders Corneal Dystrophy, Juvenile Epithelial of Meesmann Color Vision Defects Muscular Diseases Neuromuscular Diseases Nails, Malformed Corneal Opacity Keratoconus Myotonia Photophobia Cardiomyopathies Muscle Weakness Walker-Warburg Syndrome Sarcoglycanopathies

Chemicals and Drugs35

Thymopoietins Dystrophin Dystroglycans cis-trans-Isomerases Eye Proteins Peripherins Sarcoglycans Utrophin Codon, Nonsense Lipofuscin Membrane Proteins Rhodopsin Intermediate Filament Proteins Carrier Proteins Collagen Type VI Nerve Tissue Proteins Proteins Collagen Type VIII ATP-Binding Cassette Transporters Dystrophin-Associated Proteins Rod Opsins Muscle Proteins Creatine Kinase Guanylate Cyclase Lamin Type A Laminin Caveolin 3 Dystrophin-Associated Protein Complex Cytoskeletal Proteins Poly(A)-Binding Protein II RNA, Messenger Extracellular Matrix Proteins Genetic Markers Receptor Protein-Tyrosine Kinases Calpain

Analytical, Diagnostic and Therapeutic Techniques and Equipment22

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Fluorescein Angiography Chromosome Mapping Disease Models, Animal Tomography, Optical Coherence Heteroduplex Analysis Genetic Testing Polymerase Chain Reaction Visual Field Tests Ophthalmoscopy Heterozygote Detection Keratoplasty, Penetrating Sequence Analysis, DNA Amino Acid Substitution Immunohistochemistry Electrooculography Blotting, Western Genetic Therapy Reverse Transcriptase Polymerase Chain Reaction

Psychiatry and Psychology4

Visual Acuity Visual Fields Intellectual Disability Vision, Ocular

Phenomena and Processes38

Phenotype Mutation Genes, Recessive Consanguinity Genes, Dominant Visual Acuity Exons Mutation, Missense Dark Adaptation Genetic Linkage Codon, Nonsense Base Sequence Heterozygote Homozygote Genotype Visual Fields Frameshift Mutation Amino Acid Sequence Lod Score Exome Polymorphism, Single-Stranded Conformational Haplotypes Trinucleotide Repeat Expansion Point Mutation Chromosomes, Human, Pair 4 X Chromosome Alleles Amino Acid Substitution Polymorphism, Single Nucleotide Vision, Ocular Light Fluorescence Gene Deletion Genetic Markers Gene Expression Regulation Cell Differentiation Muscle Development Regeneration

Disciplines and Occupations1

Immunohistochemistry

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 Disciplines and Occupations Information Science Health Care

Retinal Dystrophies Muscular Dystrophies Thymopoietins Muscular Dystrophy, Emery-Dreifuss Myotonic Dystrophy Phenotype Dystrophin Dystroglycans Muscular Dystrophy, Duchenne Corneal Dystrophies, Hereditary Retinal Degeneration Muscular Dystrophy, Animal Leber Congenital Amaurosis Retinitis Pigmentosa Fuchs' Endothelial Dystrophy Electroretinography cis-trans-Isomerases Muscular Dystrophy, Facioscapulohumeral Pedigree Eye Proteins Fundus Oculi Mutation Genes, Recessive Consanguinity Retinal Diseases Mice, Inbred mdx Laurence-Moon Syndrome Photoreceptor Cells, Vertebrate Eye Diseases, Hereditary DNA Mutational Analysis Peripherins Retina Neuroaxonal Dystrophies Blindness Sarcoglycans Genes, Dominant Pigment Epithelium of Eye Night Blindness Bardet-Biedl Syndrome Microphthalmos Muscular Dystrophy, Oculopharyngeal Visual Acuity Photoreceptor Cells Reflex Sympathetic Dystrophy Exons Mutation, Missense Dark Adaptation Syndrome Fluorescein Angiography Utrophin Molecular Sequence Data Vitelliform Macular Dystrophy Retinal Pigment Epithelium Muscle, Skeletal Alstrom Syndrome Macular Degeneration Genetic Linkage Retinal Cone Photoreceptor Cells Retinal Rod Photoreceptor Cells Codon, Nonsense Chromosome Mapping Base Sequence Choroid Diseases Usher Syndromes Optic Atrophy, Hereditary, Leber Heterozygote Homozygote Optic Atrophies, Hereditary Genotype Kidney Diseases, Cystic Lipofuscin Age of Onset Rats, Mutant Strains Optic Disk Drusen Visual Fields Disease Models, Animal Frameshift Mutation Membrane Proteins Tomography, Optical Coherence Amino Acid Sequence Lod Score Abnormalities, Multiple Exome Heteroduplex Analysis Polymorphism, Single-Stranded Conformational Haplotypes Genetic Testing Rhodopsin Polymerase Chain Reaction Myotonic Disorders Visual Field Tests Intellectual Disability Intermediate Filament Proteins Trinucleotide Repeat Expansion Carrier Proteins Ophthalmoscopy Collagen Type VI Vision Disorders Mice, Inbred C57BL Nerve Tissue Proteins

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