Cone rod dystr genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy12

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

Organisms4

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

Diseases38

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

Chemicals and Drugs25

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment16

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

Psychiatry and Psychology5

Visual Acuity Visual Fields Vision, Ocular Intellectual Disability Color Perception

Phenomena and Processes29

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

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

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