Types retinitis pigmentosa. Medical search. Frequent questions

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Anatomy18

Photoreceptor Cells, Vertebrate Retina Fundus Oculi Photoreceptor Cells Retinal Rod Photoreceptor Cells Retinal Cone Photoreceptor Cells X Chromosome Retinal Photoreceptor Cell Outer Segment Fovea Centralis Photoreceptor Connecting Cilium Macula Lutea Cilia Rod Cell Outer Segment Retinal Bipolar Cells Retinal Pigment Epithelium Chromosomes, Human, Pair 19 Pigment Epithelium of Eye Retinal Photoreceptor Cell Inner Segment

Organisms2

Rats, Transgenic Dependovirus

Diseases24

Retinitis Pigmentosa Cytomegalovirus Retinitis Retinitis Retinal Degeneration Genetic Diseases, X-Linked Usher Syndromes Night Blindness Blindness Eye Diseases, Hereditary Laurence-Moon Syndrome Retinal Diseases Leber Congenital Amaurosis Vision Disorders Retinal Dysplasia Disease Models, Animal Optic Atrophy, Hereditary, Leber Ataxia Eye Infections, Viral Bardet-Biedl Syndrome Retinal Dystrophies Syndrome Vision, Low Optic Atrophies, Hereditary Optic Disk Drusen

Chemicals and Drugs16

Eye Proteins Rhodopsin Peripherins Cyclic Nucleotide Phosphodiesterases, Type 6 Rod Opsins IMP Dehydrogenase Carbonic Anhydrase IV Ribonucleoprotein, U4-U6 Small Nuclear Tetraspanins Intermediate Filament Proteins Opsins cis-trans-Isomerases Codon, Nonsense Foscarnet Carrier Proteins Arrestin

Analytical, Diagnostic and Therapeutic Techniques and Equipment16

Electroretinography Pedigree Visual Acuity DNA Mutational Analysis Visual Field Tests Fluorescein Angiography Tomography, Optical Coherence Chromosome Mapping Disease Models, Animal Vision Tests Sequence Analysis, DNA Ophthalmoscopy Polymerase Chain Reaction Visual Prosthesis Ophthalmoscopes Electrooculography

Psychiatry and Psychology5

Visual Acuity Visual Fields Sensory Thresholds Phosphenes Vision, Ocular

Phenomena and Processes29

Genes, Dominant Genes, Recessive Dark Adaptation Visual Acuity Visual Fields Mutation Genetic Linkage Consanguinity X Chromosome Exons Mutation, Missense Homozygote Lod Score Polymorphism, Single-Stranded Conformational Phenotype Frameshift Mutation Genes, X-Linked Phosphenes Amino Acid Sequence Heterozygote Base Sequence Codon, Nonsense Vision, Ocular Point Mutation Light Genotype RNA Splicing Chromosomes, Human, Pair 19 Genetic Heterogeneity

Information Science3

Molecular Sequence Data Amino Acid Sequence Base Sequence

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science

Retinitis Pigmentosa Cytomegalovirus Retinitis Electroretinography Eye Proteins Rhodopsin Retinitis Retinal Degeneration Photoreceptor Cells, Vertebrate Genes, Dominant Pedigree Genes, Recessive Retina Peripherins Genetic Diseases, X-Linked Dark Adaptation Fundus Oculi Visual Acuity Photoreceptor Cells Cyclic Nucleotide Phosphodiesterases, Type 6 Retinal Rod Photoreceptor Cells Visual Fields Usher Syndromes Retinal Cone Photoreceptor Cells Mutation Night Blindness Genetic Linkage DNA Mutational Analysis Rod Opsins Blindness Consanguinity Visual Field Tests X Chromosome Exons Mutation, Missense Eye Diseases, Hereditary Fluorescein Angiography Tomography, Optical Coherence IMP Dehydrogenase Homozygote Molecular Sequence Data Laurence-Moon Syndrome Retinal Diseases Carbonic Anhydrase IV Leber Congenital Amaurosis Ribonucleoprotein, U4-U6 Small Nuclear Retinal Photoreceptor Cell Outer Segment Tetraspanins Fovea Centralis Lod Score Vision Disorders Intermediate Filament Proteins Polymorphism, Single-Stranded Conformational Photoreceptor Connecting Cilium Phenotype Chromosome Mapping Sensory Thresholds Opsins Frameshift Mutation cis-trans-Isomerases Genes, X-Linked Retinal Dysplasia Macula Lutea Disease Models, Animal Optic Atrophy, Hereditary, Leber Ataxia Phosphenes Amino Acid Sequence Heterozygote Base Sequence Eye Infections, Viral Codon, Nonsense Vision Tests Vision, Ocular Bardet-Biedl Syndrome Retinal Dystrophies Syndrome Sequence Analysis, DNA Ophthalmoscopy Cilia Polymerase Chain Reaction Vision, Low Point Mutation Rats, Transgenic Visual Prosthesis Light Rod Cell Outer Segment Ophthalmoscopes Genotype Electrooculography Optic Atrophies, Hereditary Foscarnet Carrier Proteins RNA Splicing Retinal Bipolar Cells Retinal Pigment Epithelium Arrestin Chromosomes, Human, Pair 19 Pigment Epithelium of Eye Genetic Heterogeneity Dependovirus

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