Symptoms genetic genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy10

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

Organisms3

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

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

Chemicals and Drugs21

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment17

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Fluorescein Angiography Heteroduplex Analysis Tomography, Optical Coherence Visual Field Tests Chromosome Mapping Ophthalmoscopy Genetic Testing Disease Models, Animal Polymerase Chain Reaction Symptom Assessment Severity of Illness Index Questionnaires Sequence Analysis, DNA

Psychiatry and Psychology5

Visual Acuity Visual Fields Intellectual Disability Depression Vision, Ocular

Phenomena and Processes27

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

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Questionnaires

Health Care4

Age of Onset Genetic Testing Severity of Illness Index Questionnaires

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

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