Diagnosis 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

Organisms2

Mice, Inbred mdx Rats, Mutant Strains

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 Abnormalities, Multiple Reflex Sympathetic Dystrophy Muscular Dystrophy, Oculopharyngeal Vision Disorders 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 Carrier Proteins Rod Opsins Membrane Proteins Proteins ATP-Binding Cassette Transporters Guanylate Cyclase Thymopoietins Collagen Type VI Receptor Protein-Tyrosine Kinases

Analytical, Diagnostic and Therapeutic Techniques and Equipment23

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Fluorescein Angiography Prenatal Diagnosis Heteroduplex Analysis Tomography, Optical Coherence Delayed Diagnosis Visual Field Tests Chromosome Mapping Genetic Testing Polymerase Chain Reaction Early Diagnosis Ophthalmoscopy Sensitivity and Specificity Diagnosis Disease Models, Animal Retrospective Studies Biopsy Heterozygote Detection Diagnostic Errors Sequence Analysis, DNA

Psychiatry and Psychology4

Visual Acuity Visual Fields Intellectual Disability Vision, Ocular

Phenomena and Processes28

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

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care5

Age of Onset Genetic Testing Sensitivity and Specificity Retrospective Studies Diagnostic Errors

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

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