Autosomal dominant cardiac ttr amyloidosis. Medical search. Frequent questions

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Anatomy11

Myocytes, Cardiac Heart Myocardium Kidney Heart Ventricles Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 19 Cells, Cultured Chromosomes, Human, Pair 16 Myoblasts, Cardiac Chromosomes, Human, Pair 1

Organisms4

Mice, Transgenic Acinonyx Dogs Mice, Inbred C57BL

Diseases44

Amyloidosis Amyloid Neuropathies, Familial Amyloidosis, Familial Polycystic Kidney, Autosomal Dominant Amyloid Neuropathies Familial Mediterranean Fever Cardiomyopathies Retinitis Pigmentosa Arrhythmias, Cardiac Optic Atrophy, Autosomal Dominant Death, Sudden, Cardiac Heart Diseases Syndrome Polycystic Kidney Diseases Cataract CADASIL Kidney Diseases Skin Diseases, Genetic Disease Models, Animal Nephrotic Syndrome Paraproteinemias Cardiomegaly Tracheal Diseases Spinocerebellar Degenerations Cardiac Tamponade Cysts Dementia, Multi-Infarct Macroglossia Cerebellar Ataxia Heart Failure Spastic Paraplegia, Hereditary Abnormalities, Multiple Hand Deformities, Congenital Heart Arrest Chromosome Disorders Foot Deformities, Congenital Skin Diseases Corneal Dystrophies, Hereditary Nails, Malformed Hearing Loss, Sensorineural Liver Diseases Genetic Predisposition to Disease Spinocerebellar Ataxias Tuberous Sclerosis

Chemicals and Drugs21

Prealbumin Amyloid Serum Amyloid A Protein Immunoglobulin Light Chains TRPP Cation Channels Congo Red Serum Amyloid P-Component Diflunisal beta 2-Microglobulin Amyloidogenic Proteins Genetic Markers Melphalan Eye Proteins Bence Jones Protein Cardiac Myosins Immunoglobulin lambda-Chains gamma-Crystallins Gelsolin beta-Crystallin A Chain Codon, Nonsense Rhodopsin

Analytical, Diagnostic and Therapeutic Techniques and Equipment24

Pedigree Cardiac Output DNA Mutational Analysis Cardiac Surgical Procedures Chromosome Mapping Biopsy Disease Models, Animal Cardiac Pacing, Artificial Electrocardiography Polymerase Chain Reaction Cardiac Catheterization Echocardiography Treatment Outcome Fatal Outcome Amino Acid Substitution Retrospective Studies Heart Transplantation Immunohistochemistry Follow-Up Studies Genetic Testing Cardiac Imaging Techniques Heart Rate Electroretinography Prognosis

Psychiatry and Psychology1

Dementia, Multi-Infarct

Phenomena and Processes33

Genes, Dominant Mutation Genetic Linkage Cardiac Output Lod Score Mutation, Missense Phenotype Heterozygote Base Sequence Time Factors Haplotypes Penetrance Amino Acid Sequence Genetic Heterogeneity Genetic Markers Genes, Recessive Genotype Exons Point Mutation Myocardial Contraction Frameshift Mutation Chromosomes, Human, Pair 2 Amino Acid Substitution Alleles Microsatellite Repeats Homozygote Chromosomes, Human, Pair 19 Polymorphism, Single-Stranded Conformational Chromosomes, Human, Pair 16 Genetic Predisposition to Disease Codon, Nonsense Heart Rate Chromosomes, Human, Pair 1

Disciplines and Occupations1

Immunohistochemistry

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Fatal Outcome

Health Care7

Age of Onset Family Health Treatment Outcome Fatal Outcome Retrospective Studies Follow-Up Studies Genetic Testing

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

Prealbumin Amyloidosis Amyloid Neuropathies, Familial Amyloidosis, Familial Genes, Dominant Polycystic Kidney, Autosomal Dominant Pedigree Amyloid Serum Amyloid A Protein Amyloid Neuropathies Myocytes, Cardiac Mutation Genetic Linkage Familial Mediterranean Fever Cardiac Output Cardiomyopathies Immunoglobulin Light Chains TRPP Cation Channels Lod Score Heart Retinitis Pigmentosa DNA Mutational Analysis Mutation, Missense Phenotype Arrhythmias, Cardiac Optic Atrophy, Autosomal Dominant Congo Red Molecular Sequence Data Cardiac Surgical Procedures Death, Sudden, Cardiac Heart Diseases Chromosome Mapping Syndrome Myocardium Serum Amyloid P-Component Diflunisal Heterozygote Polycystic Kidney Diseases Cataract beta 2-Microglobulin CADASIL Kidney Diseases Base Sequence Amyloidogenic Proteins Skin Diseases, Genetic Age of Onset Time Factors Haplotypes Biopsy Disease Models, Animal Nephrotic Syndrome Kidney Penetrance Paraproteinemias Family Health Cardiomegaly Amino Acid Sequence Tracheal Diseases Spinocerebellar Degenerations Genetic Heterogeneity Cardiac Pacing, Artificial Mice, Transgenic Genetic Markers Cardiac Tamponade Genes, Recessive Genotype Exons Point Mutation Cysts Dementia, Multi-Infarct Electrocardiography Macroglossia Cerebellar Ataxia Myocardial Contraction Heart Ventricles Polymerase Chain Reaction Cardiac Catheterization Echocardiography Frameshift Mutation Treatment Outcome Melphalan Fatal Outcome Eye Proteins Heart Failure Spastic Paraplegia, Hereditary Chromosomes, Human, Pair 2 Abnormalities, Multiple Hand Deformities, Congenital Bence Jones Protein Heart Arrest Acinonyx Amino Acid Substitution Chromosome Disorders Alleles Cardiac Myosins Retrospective Studies Microsatellite Repeats Heart Transplantation Homozygote Immunoglobulin lambda-Chains

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