Cone dystrophy genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy18

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

Organisms2

Mice, Inbred mdx Rats, Mutant Strains

Diseases41

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

Chemicals and Drugs26

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment16

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

Psychiatry and Psychology5

Visual Acuity Visual Fields Sensory Thresholds Vision, Ocular Intellectual Disability

Phenomena and Processes28

X Chromosome Dark Adaptation Visual Acuity Genes, Dominant Mutation Consanguinity Genes, Recessive Mutation, Missense Phenotype Genetic Linkage Visual Fields Exons Codon, Nonsense Heterozygote Homozygote Base Sequence Frameshift Mutation Lod Score Exome Vision, Ocular Polymorphism, Single-Stranded Conformational Haplotypes Trinucleotide Repeat Expansion Genotype Light Amino Acid Sequence Chromosomes, Human, Pair 4 Point Mutation

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

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