Traits genes autosomal dominant disease huntington disease. Medical search. Frequent questions

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Anatomy10

Chromosomes, Human, Pair 4 Corpus Striatum Brain Caudate Nucleus Neostriatum Inclusion Bodies Neurons Nerve Fibers, Unmyelinated Putamen Cerebral Cortex

Organisms2

Rats, Transgenic Mice, Transgenic

Diseases21

Huntington Disease Telangiectasia, Hereditary Hemorrhagic Polycystic Kidney, Autosomal Dominant Genetic Diseases, Inborn Protoporphyria, Erythropoietic Disease Models, Animal Muscular Dystrophy, Facioscapulohumeral Chorea Prodromal Symptoms Neurodegenerative Diseases Atrophy Retinitis Pigmentosa Disease Progression Optic Atrophy, Autosomal Dominant Genetic Predisposition to Disease Polycystic Kidney Diseases Cataract CADASIL Nerve Degeneration Syndrome Spinocerebellar Degenerations

Chemicals and Drugs13

Nerve Tissue Proteins Genetic Markers Nuclear Proteins Quinolinic Acid 3-Hydroxyanthranilate 3,4-Dioxygenase Tetrabenazine TRPP Cation Channels Quinolinic Acids Peptides Mutant Proteins Dopamine and cAMP-Regulated Phosphoprotein 32 Nitro Compounds DNA

Analytical, Diagnostic and Therapeutic Techniques and Equipment18

Pedigree Chromosome Mapping DNA Mutational Analysis Polymerase Chain Reaction Crosses, Genetic Models, Genetic Genetic Testing Disease Models, Animal Prodromal Symptoms Witchcraft Rotarod Performance Test Gene Knock-In Techniques Chromosome Banding Heterozygote Detection Magnetic Resonance Imaging Early Diagnosis Severity of Illness Index Longitudinal Studies

Psychiatry and Psychology5

Huntington Disease Family Cognition Disorders Neuropsychological Tests Motor Activity

Phenomena and Processes29

Genes, Dominant Mutation Phenotype Genetic Linkage Quantitative Trait Loci Mutation, Missense Quantitative Trait, Heritable Trinucleotide Repeat Expansion Trinucleotide Repeats Chromosomes, Human, Pair 4 Base Sequence Genetic Markers Alleles Heterozygote Genes, Recessive Genotype Exons Haplotypes Lod Score Homozygote Point Mutation Lipoylation Genetic Predisposition to Disease Polymorphism, Restriction Fragment Length Gene Frequency Genetic Heterogeneity Autophagy Penetrance Motor Activity

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Witchcraft Family

Humanities1

Information Science2

Base Sequence Molecular Sequence Data

Health Care7

Genetic Testing Age of Onset Genetic Counseling Family Health Age Factors Severity of Illness Index Longitudinal Studies

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 Humanities Information Science Health Care

Huntington Disease Genes, Dominant Pedigree Telangiectasia, Hereditary Hemorrhagic Mutation Phenotype Genetic Linkage Quantitative Trait Loci Mutation, Missense Quantitative Trait, Heritable Trinucleotide Repeat Expansion Chromosome Mapping DNA Mutational Analysis Trinucleotide Repeats Chromosomes, Human, Pair 4 Base Sequence Nerve Tissue Proteins Molecular Sequence Data Polycystic Kidney, Autosomal Dominant Polymerase Chain Reaction Crosses, Genetic Genetic Diseases, Inborn Models, Genetic Genetic Testing Genetic Markers Age of Onset Protoporphyria, Erythropoietic Nuclear Proteins Disease Models, Animal Alleles Quinolinic Acid Heterozygote Muscular Dystrophy, Facioscapulohumeral Genes, Recessive Corpus Striatum Chorea 3-Hydroxyanthranilate 3,4-Dioxygenase Genotype Rats, Transgenic Prodromal Symptoms Exons Neurodegenerative Diseases Mice, Transgenic Witchcraft Haplotypes Brain Atrophy Caudate Nucleus Rotarod Performance Test Lod Score Homozygote Neostriatum Tetrabenazine Mythology TRPP Cation Channels Quinolinic Acids Point Mutation Peptides Retinitis Pigmentosa Mutant Proteins Inclusion Bodies Neurons Nerve Fibers, Unmyelinated Gene Knock-In Techniques Genetic Counseling Chromosome Banding Disease Progression Putamen Optic Atrophy, Autosomal Dominant Dopamine and cAMP-Regulated Phosphoprotein 32 Lipoylation Family Heterozygote Detection Genetic Predisposition to Disease Magnetic Resonance Imaging Polymorphism, Restriction Fragment Length Early Diagnosis Nitro Compounds Family Health Polycystic Kidney Diseases Cataract DNA CADASIL Nerve Degeneration Syndrome Cognition Disorders Age Factors Gene Frequency Severity of Illness Index Longitudinal Studies Genetic Heterogeneity Autophagy Penetrance Cerebral Cortex Neuropsychological Tests Motor Activity Spinocerebellar Degenerations

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