Vitelliform dystrophy diseases genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy19

Fundus Oculi Macula Lutea Pigment Epithelium of Eye Photoreceptor Cells, Vertebrate Retina Chromosomes, Human, Pair 11 Photoreceptor Cells Retinal Pigment Epithelium Muscle, Skeletal Retinal Cone Photoreceptor Cells Retinal Rod Photoreceptor Cells Chromosomes, Human, Pair 4 X Chromosome Myoblasts Cornea Muscles Sarcolemma Muscle Fibers, Skeletal Rod Cell Outer Segment

Organisms3

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

Diseases45

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

Chemicals and Drugs26

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment18

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

Psychiatry and Psychology4

Visual Acuity Intellectual Disability Visual Fields Huntington Disease

Phenomena and Processes34

Visual Acuity Mutation Genes, Recessive Consanguinity Exons Genetic Linkage Genes, Dominant Phenotype Chromosomes, Human, Pair 11 Mutation, Missense Lod Score Dark Adaptation Exome Haplotypes Codon, Nonsense Homozygote Heterozygote Genetic Markers Base Sequence Trinucleotide Repeat Expansion Chromosomes, Human, Pair 4 Genotype Frameshift Mutation Polymorphism, Single-Stranded Conformational Visual Fields Amino Acid Sequence X Chromosome Genetic Predisposition to Disease Polymorphism, Single Nucleotide Point Mutation Genome, Human Alleles Genetic Heterogeneity Linkage Disequilibrium

Disciplines and Occupations1

Computational Biology

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Databases, Genetic

Health Care2

Genetic Testing Age of Onset

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

Vitelliform Macular Dystrophy Retinal Dystrophies Muscular Dystrophies Myotonic Dystrophy Muscular Dystrophy, Duchenne Retinal Degeneration Paraneoplastic Syndromes, Ocular Eye Proteins Electrooculography Corneal Dystrophies, Hereditary Eye Diseases, Hereditary Macular Degeneration Pedigree Electroretinography Fluorescein Angiography Muscular Dystrophy, Animal Fundus Oculi Retinal Diseases Leber Congenital Amaurosis Chloride Channels Retinitis Pigmentosa Fuchs' Endothelial Dystrophy Visual Acuity Macula Lutea cis-trans-Isomerases Muscular Dystrophy, Facioscapulohumeral Dystrophin Mutation Pigment Epithelium of Eye Genes, Recessive Consanguinity Tomography, Optical Coherence Genetic Diseases, Inborn Exons Muscular Dystrophy, Emery-Dreifuss DNA Mutational Analysis Genetic Linkage Mice, Inbred mdx Laurence-Moon Syndrome Photoreceptor Cells, Vertebrate Retina Peripherins Chromosome Mapping Genes, Dominant Phenotype Neuroaxonal Dystrophies Disease Blindness Sarcoglycans Chromosomes, Human, Pair 11 Night Blindness Mutation, Missense Bardet-Biedl Syndrome Muscular Dystrophy, Oculopharyngeal Lod Score Dystroglycans Reflex Sympathetic Dystrophy Photoreceptor Cells Syndrome Microphthalmos Dark Adaptation Exome Utrophin Alstrom Syndrome Retinal Pigment Epithelium Haplotypes Molecular Sequence Data Muscle, Skeletal Codon, Nonsense Retinal Cone Photoreceptor Cells Homozygote Retinal Rod Photoreceptor Cells Heterozygote Kidney Diseases, Cystic Genetic Testing Genetic Markers Base Sequence Choroid Diseases Optic Atrophy, Hereditary, Leber Usher Syndromes Nerve Tissue Proteins Age of Onset Optic Atrophies, Hereditary Trinucleotide Repeat Expansion Chromosomes, Human, Pair 4 Genotype Frameshift Mutation Lipofuscin Polymorphism, Single-Stranded Conformational Optic Disk Drusen Intellectual Disability Proteins Visual Fields Rats, Mutant Strains Abnormalities, Multiple Heterozygote Detection Disease Models, Animal Membrane Proteins Heteroduplex Analysis Polymerase Chain Reaction

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