Alterations hereditary genes cases retinal dystrophies. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy10

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

Organisms4

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

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 Muscular Dystrophy, Emery-Dreifuss Syndrome Usher Syndromes Optic Atrophy, Hereditary, Leber Macular Degeneration Choroid Diseases Neuroaxonal Dystrophies Optic Atrophies, Hereditary Optic Disk Drusen Kidney Diseases, Cystic Muscular Dystrophy, Oculopharyngeal Reflex Sympathetic Dystrophy Vision Disorders Abnormalities, Multiple Vitelliform Macular Dystrophy Disease Models, Animal Intellectual Disability Myotonic Disorders

Chemicals and Drugs21

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Fluorescein Angiography Heteroduplex Analysis Tomography, Optical Coherence Chromosome Mapping Visual Field Tests Ophthalmoscopy Disease Models, Animal Genetic Testing Polymerase Chain Reaction Sequence Analysis, DNA Amino Acid Substitution

Psychiatry and Psychology4

Visual Acuity Visual Fields Intellectual Disability Vision, Ocular

Phenomena and Processes29

Consanguinity Genes, Recessive Mutation Dark Adaptation Visual Acuity Phenotype Genes, Dominant Mutation, Missense Exons Codon, Nonsense Visual Fields Genetic Linkage Exome Polymorphism, Single-Stranded Conformational Homozygote Base Sequence Heterozygote Frameshift Mutation Lod Score Haplotypes Amino Acid Sequence Genotype Point Mutation Vision, Ocular Light Fluorescence Amino Acid Substitution Trinucleotide Repeat Expansion Polymorphism, Single Nucleotide

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

No FAQ available that match "alterations hereditary genes cases retinal dystrophies"