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

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Anatomy25

Cornea X Chromosome Descemet Membrane Muscles Fundus Oculi Endothelium, Corneal Bowman Membrane Corneal Stroma Photoreceptor Cells, Vertebrate Retina Muscle, Skeletal Pigment Epithelium of Eye Chromosomes, Human, Pair 5 Photoreceptor Cells Epithelium, Corneal Retinal Cone Photoreceptor Cells Retinal Pigment Epithelium Retinal Rod Photoreceptor Cells Corneal Keratocytes Chromosomes, Human, Pair 20 Myoblasts Sarcolemma Chromosomes, Human, Pair 4 Muscle Fibers, Skeletal Basement Membrane

Organisms3

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

Diseases50

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

Chemicals and Drugs45

Dystrophin Collagen Type VIII Eye Proteins cis-trans-Isomerases Keratin-12 Extracellular Matrix Proteins Keratan Sulfate Sarcoglycans Peripherins Dystroglycans Utrophin Transforming Growth Factor beta Dimethylallyltranstransferase Keratin-3 Sulfotransferases Codon, Nonsense Thymopoietins Collagen Type VI Lipofuscin Dystrophin-Associated Proteins Membrane Proteins Creatine Kinase Anion Transport Proteins Muscle Proteins Intermediate Filament Proteins Rhodopsin Genetic Markers Transforming Growth Factor beta1 Nerve Tissue Proteins Lamin Type A Laminin Caveolin 3 Carrier Proteins Dystrophin-Associated Protein Complex Amyloid Proteins Poly(A)-Binding Protein II Homeodomain Proteins Rod Opsins ATP-Binding Cassette Transporters Basic Helix-Loop-Helix Leucine Zipper Transcription Factors Antiporters Decorin Guanylate Cyclase Collagen Type IV

Analytical, Diagnostic and Therapeutic Techniques and Equipment26

Pedigree Electroretinography DNA Mutational Analysis Keratoplasty, Penetrating Visual Acuity Corneal Transplantation Corneal Pachymetry Fluorescein Angiography Polymerase Chain Reaction Chromosome Mapping Photorefractive Keratectomy Lasers, Excimer Tomography, Optical Coherence Genetic Testing Amino Acid Substitution Corneal Topography Microscopy, Confocal Heterozygote Detection Disease Models, Animal Sequence Analysis, DNA Ophthalmoscopy Heteroduplex Analysis Visual Field Tests Genetic Association Studies Blotting, Western Immunohistochemistry

Psychiatry and Psychology4

Visual Acuity Visual Fields Intellectual Disability Family

Phenomena and Processes32

X Chromosome Mutation Consanguinity Mutation, Missense Exons Phenotype Genes, Recessive Genes, Dominant Heterozygote Visual Acuity Genetic Linkage Homozygote Base Sequence Chromosomes, Human, Pair 5 Dark Adaptation Frameshift Mutation Polymorphism, Single-Stranded Conformational Haplotypes Lod Score Point Mutation Codon, Nonsense Genotype Amino Acid Substitution Trinucleotide Repeat Expansion Chromosomes, Human, Pair 20 Visual Fields Amino Acid Sequence Chromosomes, Human, Pair 4 Exome Genetic Heterogeneity Genetic Markers Polymorphism, Single Nucleotide

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Current Procedural Terminology Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups1

Asian Continental Ancestry Group

Health Care2

Genetic Testing Age of Onset

Geographicals1

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care Geographicals

Corneal Dystrophies, Hereditary Retinal Dystrophies Muscular Dystrophies Myotonic Dystrophy Dystrophin Fuchs' Endothelial Dystrophy Muscular Dystrophy, Duchenne Corneal Dystrophy, Juvenile Epithelial of Meesmann Muscular Dystrophy, Animal Collagen Type VIII Retinal Degeneration Pedigree Cornea Leber Congenital Amaurosis Muscular Dystrophy, Facioscapulohumeral X Chromosome Retinitis Pigmentosa Electroretinography Corneal Opacity Eye Proteins DNA Mutational Analysis Descemet Membrane Muscles Mutation cis-trans-Isomerases Fundus Oculi Keratin-12 Extracellular Matrix Proteins Muscular Dystrophy, Emery-Dreifuss Endothelium, Corneal Mice, Inbred mdx Keratoplasty, Penetrating Consanguinity Bowman Membrane Keratoconus Neuroaxonal Dystrophies Mutation, Missense Exons Phenotype Keratan Sulfate Sarcoglycans Genes, Recessive Corneal Stroma Amyloidosis, Familial Genes, Dominant Retinal Diseases Heterozygote Visual Acuity Photoreceptor Cells, Vertebrate Corneal Transplantation Eye Diseases, Hereditary Laurence-Moon Syndrome Peripherins Muscular Dystrophy, Oculopharyngeal Dystroglycans Genetic Linkage Reflex Sympathetic Dystrophy Retina Corneal Pachymetry Corneal Diseases Utrophin Vitelliform Macular Dystrophy Current Procedural Terminology Blindness Transforming Growth Factor beta Homozygote Muscle, Skeletal Dimethylallyltranstransferase Molecular Sequence Data Keratin-3 Base Sequence Night Blindness Pigment Epithelium of Eye Corneal Edema Macular Degeneration Chromosomes, Human, Pair 5 Sulfotransferases Fluorescein Angiography Polymerase Chain Reaction Photoreceptor Cells Dark Adaptation Bardet-Biedl Syndrome Epithelium, Corneal Frameshift Mutation Polymorphism, Single-Stranded Conformational Microphthalmos Chromosome Mapping Photorefractive Keratectomy Retinal Cone Photoreceptor Cells Retinal Pigment Epithelium Syndrome Haplotypes Lod Score Alstrom Syndrome Point Mutation Retinal Rod Photoreceptor Cells Lasers, Excimer Corneal Keratocytes Tomography, Optical Coherence Codon, Nonsense

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