Inherited disorder genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy15

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 X Chromosome Rod Cell Outer Segment Fibroblasts Cells, Cultured Cell Line Skin

Organisms6

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

Diseases64

Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Muscular Dystrophy, Duchenne Retinitis Pigmentosa Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Syndrome Genetic Diseases, Inborn Fuchs' Endothelial Dystrophy Retinal Diseases Protoporphyria, Erythropoietic Laurence-Moon Syndrome Metabolism, Inborn Errors Eye Diseases, Hereditary Blindness Muscular Dystrophy, Facioscapulohumeral Granulomatous Disease, Chronic Bardet-Biedl Syndrome Microphthalmos Night Blindness Alstrom Syndrome Abnormalities, Multiple Porphyria, Hepatoerythropoietic Muscular Dystrophy, Emery-Dreifuss Disease Models, Animal Jaundice, Chronic Idiopathic Intellectual Disability Amino Acid Metabolism, Inborn Errors Usher Syndromes Optic Atrophy, Hereditary, Leber Lipid Metabolism, Inborn Errors Hepatolenticular Degeneration Macular Degeneration Hemochromatosis Neuroaxonal Dystrophies Choroid Diseases Optic Atrophies, Hereditary Ichthyosis Optic Disk Drusen Hypophosphatasia Kidney Diseases, Cystic Hemoglobinopathies Gitelman Syndrome Ichthyosiform Erythroderma, Congenital Vision Disorders Muscular Dystrophy, Oculopharyngeal Tooth Abnormalities Reflex Sympathetic Dystrophy Purine-Pyrimidine Metabolism, Inborn Errors Myasthenic Syndromes, Congenital Photosensitivity Disorders Vitelliform Macular Dystrophy Genetic Predisposition to Disease Refsum Disease Familial Mediterranean Fever Adrenoleukodystrophy Malignant Hyperthermia Substance-Related Disorders Long QT Syndrome Myotonic Disorders Tic Disorders

Chemicals and Drugs26

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment19

Pedigree Electroretinography DNA Mutational Analysis Chromosome Mapping Genetic Testing Visual Acuity Fluorescein Angiography Disease Models, Animal Polymerase Chain Reaction Heterozygote Detection Heteroduplex Analysis Prenatal Diagnosis Tomography, Optical Coherence Visual Field Tests Ophthalmoscopy Genetic Therapy Sequence Analysis, DNA Gene Transfer Techniques Amino Acid Substitution

Psychiatry and Psychology22

Bipolar Disorder Visual Acuity Mental Disorders Anxiety Disorders Mood Disorders Intellectual Disability Visual Fields Depressive Disorder, Major Attention Deficit Disorder with Hyperactivity Depressive Disorder Obsessive-Compulsive Disorder Stress Disorders, Post-Traumatic Autistic Disorder Phobic Disorders Child Development Disorders, Pervasive Psychotic Disorders Substance-Related Disorders Vision, Ocular Conduct Disorder Tic Disorders Psychiatric Status Rating Scales Cognition Disorders

Phenomena and Processes40

Mutation Genes, Recessive Consanguinity Phenotype Genes, Dominant Mutation, Missense Codon, Nonsense Heterozygote Genetic Linkage Exons Homozygote Frameshift Mutation Base Sequence Visual Acuity Dark Adaptation Genotype Lod Score Polymorphism, Single-Stranded Conformational Point Mutation Haplotypes Amino Acid Sequence Visual Fields Exome X Chromosome Genetic Predisposition to Disease Alleles Genetic Markers Vision, Ocular Sequence Deletion Trinucleotide Repeat Expansion Polymorphism, Genetic Genetic Vectors Light Polymorphism, Single Nucleotide Polymorphism, Restriction Fragment Length Gene Expression Fluorescence Gene Deletion Amino Acid Substitution Germ-Line Mutation

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Diagnostic and Statistical Manual of Mental Disorders

Named Groups1

Infant, Newborn

Health Care3

Genetic Testing Age of Onset Family Health

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Named Groups Health Care

Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Muscular Dystrophy, Duchenne Pedigree Retinitis Pigmentosa Corneal Dystrophies, Hereditary Electroretinography cis-trans-Isomerases Mutation Genes, Recessive Muscular Dystrophy, Animal Eye Proteins Fundus Oculi DNA Mutational Analysis Syndrome Genetic Diseases, Inborn Consanguinity Fuchs' Endothelial Dystrophy Retinal Diseases Protoporphyria, Erythropoietic Laurence-Moon Syndrome Phenotype Genes, Dominant Metabolism, Inborn Errors Eye Diseases, Hereditary Photoreceptor Cells, Vertebrate Retina Peripherins Blindness Mutation, Missense Muscular Dystrophy, Facioscapulohumeral Dystrophin Codon, Nonsense Heterozygote Genetic Linkage Exons Bipolar Disorder Granulomatous Disease, Chronic Molecular Sequence Data Bardet-Biedl Syndrome Pigment Epithelium of Eye Homozygote Microphthalmos Photoreceptor Cells Night Blindness Chromosome Mapping Frameshift Mutation Ferrochelatase Genetic Testing Alstrom Syndrome Base Sequence Visual Acuity Dark Adaptation Retinal Pigment Epithelium Mental Disorders Age of Onset Abnormalities, Multiple Porphyria, Hepatoerythropoietic Muscular Dystrophy, Emery-Dreifuss Genotype Anxiety Disorders Mood Disorders Fluorescein Angiography Mice, Inbred mdx Disease Models, Animal Jaundice, Chronic Idiopathic Retinal Rod Photoreceptor Cells Intellectual Disability Lod Score Amino Acid Metabolism, Inborn Errors Usher Syndromes Optic Atrophy, Hereditary, Leber Lipid Metabolism, Inborn Errors Hepatolenticular Degeneration Polymorphism, Single-Stranded Conformational Macular Degeneration Retinal Cone Photoreceptor Cells Hemochromatosis Neuroaxonal Dystrophies Choroid Diseases Optic Atrophies, Hereditary Ichthyosis Point Mutation Haplotypes Membrane Proteins Polymerase Chain Reaction Amino Acid Sequence Sarcoglycans Optic Disk Drusen Hypophosphatasia Kidney Diseases, Cystic Rats, Mutant Strains Lipofuscin Heterozygote Detection Hemoglobinopathies Carrier Proteins Diagnostic and Statistical Manual of Mental Disorders

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