Genetic diseases affecting horses. Medical search. Frequent questions

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Anatomy16

Hoof and Claw Chromosomes, Human Cell Line Cells, Cultured Liver X Chromosome Fetus Chromosomes, Human, Pair 16 Fibroblasts Carpus, Animal HeLa Cells Cilia Spermatozoa Muscle, Skeletal Induced Pluripotent Stem Cells Metacarpus

Organisms22

Equidae African horse sickness virus Perissodactyla Dependovirus Infectious Anemia Virus, Equine Dogs Mice, Inbred CFTR Strongyloidea Streptococcus equi Mice, Knockout Aesculus Ceratopogonidae Mice, Transgenic Herpesvirus 1, Equid Rhodococcus equi Mice, Inbred C57BL Ehrlichia Influenza A Virus, H3N8 Subtype Animals, Domestic Zebrafish Retroviridae Mice, Mutant Strains

Diseases52

Genetic Diseases, Inborn Genetic Diseases, Y-Linked Rare Diseases Disease Cystic Fibrosis Genetic Diseases, X-Linked Metabolism, Inborn Errors Genetic Predisposition to Disease Lameness, Animal Disease Models, Animal Sphingolipidoses Fanconi Anemia Colic Chromosome Disorders Tay-Sachs Disease Tuberous Sclerosis Muscular Dystrophy, Duchenne Dysautonomia, Familial Lipid Metabolism Disorders Equine Infectious Anemia Hemochromatosis Homocystinuria Hemophilia B beta-Thalassemia Syndrome Phenylketonurias alpha 1-Antitrypsin Deficiency Chromosome Aberrations Muscular Dystrophies Mucopolysaccharidosis I Mitochondrial Diseases Polycystic Kidney Diseases Congenital Abnormalities Kallmann Syndrome Polycystic Kidney, Autosomal Dominant Hemophilia A Kartagener Syndrome Muscular Atrophy, Spinal Neoplasms Ataxia Telangiectasia Huntington Disease Intellectual Disability Abnormalities, Multiple Myotonic Dystrophy Down Syndrome Hematologic Diseases Genomic Instability Retinitis Pigmentosa Anemia, Sickle Cell Thalassemia Rickettsiaceae Infections West Nile Fever

Chemicals and Drugs35

Cystic Fibrosis Transmembrane Conductance Regulator Codon, Nonsense DNA Genetic Markers Factor IX Dystrophin Steroid 21-Hydroxylase TRPP Cation Channels Codon, Terminator Survival of Motor Neuron 1 Protein Cystathionine beta-Synthase Proteins Neurofibromin 1 Fanconi Anemia Complementation Group Proteins Ethylnitrosourea DNA Primers Membrane Proteins RNA Splice Sites RNA, Messenger alpha 1-Antitrypsin Phenylalanine Hydroxylase Aminoglycosides Globins DNA, Mitochondrial DNA-Binding Proteins Oligonucleotide Probes Tumor Suppressor Proteins Oligonucleotides Cytochrome c Group DNA, Complementary Xylazine Nucleotides RNA Chloride Channels Nuclear Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment37

Genetic Testing Models, Genetic Genetic Therapy Chromosome Mapping Prenatal Diagnosis Pedigree Polymerase Chain Reaction Disease Models, Animal Targeted Gene Repair DNA Mutational Analysis Genetic Techniques Preimplantation Diagnosis Gene Transfer Techniques Heterozygote Detection Sequence Analysis, DNA Gene Targeting Models, Biological Sequence Alignment Genetic Association Studies Oligonucleotide Array Sequence Analysis Cloning, Molecular Gene Expression Profiling Karyotyping Amino Acid Substitution Genome-Wide Association Study Euthanasia, Animal Models, Molecular Models, Statistical Reproducibility of Results In Situ Hybridization, Fluorescence Transfection Breeding Drug Delivery Systems Models, Animal Reverse Transcriptase Polymerase Chain Reaction Blotting, Southern Nucleic Acid Hybridization

Psychiatry and Psychology3

Huntington Disease Intellectual Disability Family

Phenomena and Processes82

Mutation Genome, Human Phenotype Base Sequence Codon, Nonsense Genetic Predisposition to Disease Alleles Genes, Recessive Nonsense Mediated mRNA Decay Genotype Genetic Vectors Polymorphism, Single Nucleotide Genetic Linkage Genetic Variation Exons Genetic Markers Heterozygote Trinucleotide Repeats Mutation, Missense Chromosomes, Human Exome Point Mutation Genome Pregnancy Chromosome Aberrations Amino Acid Sequence Gene Frequency Penetrance Physical Conditioning, Animal Haploinsufficiency Genes, Dominant Alu Elements Homozygote Founder Effect Consanguinity Codon, Terminator Evolution, Molecular Trinucleotide Repeat Expansion Algorithms Haplotypes Gene Expression Inheritance Patterns Recombination, Genetic DNA Repair Species Specificity RNA Splice Sites Introns Mutation Rate RNA Splicing Polymorphism, Genetic Gene Expression Regulation Gene Deletion Sequence Deletion X Chromosome Protein Binding Genes Microsatellite Repeats Germ-Line Mutation Polymorphism, Restriction Fragment Length Chromosomes, Human, Pair 16 Amino Acid Substitution Phylogeny Protein Structure, Tertiary Signal Transduction Mosaicism Transgenes Alternative Splicing Protein Interaction Maps Time Factors Genomic Instability Repetitive Sequences, Nucleic Acid Multigene Family Gene Dosage Transcription, Genetic Transfection DNA Damage Protein Conformation Breeding Gene Duplication Kinetics Nucleic Acid Hybridization Binding Sites

Disciplines and Occupations7

Genetics, Medical Genetic Counseling Human Genome Project Molecular Biology Computational Biology Genomics Genetics, Population

Anthropology, Education, Sociology and Social Phenomena1

Technology, Industry, Agriculture1

Humanities3

Eugenics Judaism Ethics, Medical

Information Science12

Molecular Sequence Data Base Sequence Probability Theory Human Genome Project Databases, Genetic Amino Acid Sequence Software Algorithms Databases, Nucleic Acid Internet Phylogeny Information Storage and Retrieval

Named Groups2

Jews Infant, Newborn

Health Care8

Genetic Testing Genetic Counseling Ethics, Medical Genome-Wide Association Study Euthanasia, Animal Models, Statistical Reproducibility of Results Age of Onset

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

Genetic Diseases, Inborn Mutation Eugenics Genetics, Medical Genetic Diseases, Y-Linked Rare Diseases Genome, Human Disease Genetic Testing Cystic Fibrosis Cystic Fibrosis Transmembrane Conductance Regulator Genetic Counseling Genetic Diseases, X-Linked Phenotype Models, Genetic Genetic Therapy Judaism Molecular Sequence Data Base Sequence Codon, Nonsense Metabolism, Inborn Errors Equidae Chromosome Mapping Prenatal Diagnosis African horse sickness virus Pedigree Genetic Predisposition to Disease Alleles Genes, Recessive Probability Theory Polymerase Chain Reaction Human Genome Project Nonsense Mediated mRNA Decay Genotype Lameness, Animal Disease Models, Animal Molecular Biology Sphingolipidoses Targeted Gene Repair DNA DNA Mutational Analysis Fanconi Anemia Colic Genetic Techniques Genetic Vectors Polymorphism, Single Nucleotide Preimplantation Diagnosis Gene Transfer Techniques Chromosome Disorders Tay-Sachs Disease Genetic Linkage Genetic Variation Exons Heterozygote Detection Genetic Markers Heterozygote Tuberous Sclerosis Muscular Dystrophy, Duchenne Sequence Analysis, DNA Trinucleotide Repeats Factor IX Dysautonomia, Familial Lipid Metabolism Disorders Equine Infectious Anemia Hemochromatosis Mutation, Missense Hoof and Claw Homocystinuria Perissodactyla Hemophilia B beta-Thalassemia Chromosomes, Human Exome Syndrome Point Mutation Dependovirus Databases, Genetic Phenylketonurias Dystrophin Genome alpha 1-Antitrypsin Deficiency Cell Line Pregnancy Chromosome Aberrations Computational Biology Amino Acid Sequence Gene Frequency Penetrance Physical Conditioning, Animal Steroid 21-Hydroxylase Muscular Dystrophies Gene Targeting Models, Biological Haploinsufficiency Genes, Dominant Alu Elements Homozygote Mucopolysaccharidosis I Mitochondrial Diseases Polycystic Kidney Diseases

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