Rare genetic disorders genetic hyperlipidemia. Medical search. Frequent questions

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Anatomy6

Liver Brain Cells, Cultured Cell Line Fibroblasts Chromosomes, Human, Pair 22

Organisms6

Mice, Inbred C57BL Mice, Knockout Gynostemma Mice, Transgenic Mice, Mutant Strains Gadiformes

Diseases90

Rare Diseases Progeria Myositis Ossificans Hyperlipidemia, Familial Combined Syndrome Hyperlipidemias Genetic Diseases, Inborn Hypertriglyceridemia Williams Syndrome Bone Diseases, Developmental Disease Models, Animal Musculoskeletal Abnormalities Hyperlipoproteinemia Type IV Metabolism, Inborn Errors Hypercholesterolemia Hyperlipoproteinemia Type II Prader-Willi Syndrome Xanthomatosis Genetic Predisposition to Disease Iron Metabolism Disorders Substance-Related Disorders Arteriosclerosis Ataxia Telangiectasia Neurofibromatosis 1 Chromosome Disorders Obesity Abnormalities, Multiple Pachyonychia Congenita Ectodermal Dysplasia Bloom Syndrome Tuberous Sclerosis Chondrodysplasia Punctata Tic Disorders Atherosclerosis Hyperlipoproteinemia Type III Fanconi Anemia Noonan Syndrome Skin Diseases, Genetic Ossification, Heterotopic Cockayne Syndrome Diabetes Mellitus Hypertension Nervous System Diseases Hair Diseases Sleep Disorders Insulin Resistance Body Weight 22q11 Deletion Syndrome Intellectual Disability Fatty Liver Dyslipidemias Kallmann Syndrome Diabetes Mellitus, Type 2 Lysosomal Storage Diseases Hyperlipoproteinemias Cardiovascular Diseases Metal Metabolism, Inborn Errors Turner Syndrome Lymphoproliferative Disorders Marfan Syndrome Nephrotic Syndrome alpha 1-Antitrypsin Deficiency Osteogenesis Imperfecta Huntington Disease Alcohol-Related Disorders Movement Disorders Hyperlipoproteinemia Type V Myotonic Dystrophy Microcephaly Hemochromatosis beta-Thalassemia Lipid Metabolism, Inborn Errors Speech Disorders Hepatolenticular Degeneration Chromosome Aberrations Muscular Dystrophies Acrodermatitis Down Syndrome Hydranencephaly Menkes Kinky Hair Syndrome Cystic Fibrosis Hyperglycemia Metabolic Diseases Werner Syndrome Hypohidrosis Bardet-Biedl Syndrome Craniofacial Abnormalities Dysautonomia, Familial Hyperlipoproteinemia Type I Xeroderma Pigmentosum

Chemicals and Drugs55

Triglycerides Hypolipidemic Agents Lipids Cholesterol Cholesterol, LDL Lipoproteins Apolipoproteins E Apolipoproteins B Cholesterol, HDL Apolipoproteins C Apolipoprotein E2 Apolipoprotein C-III Lipoprotein Lipase Fenofibrate Lipoproteins, VLDL Anticholesteremic Agents Neurofibromin 1 Hydroxymethylglutaryl-CoA Reductase Inhibitors Apolipoproteins Lipoproteins, LDL Cholesterol, VLDL Receptors, LDL Dietary Fats Poloxamer RecQ Helicases Heptanoic Acids Blood Glucose RNA, Messenger Apolipoprotein A-I Codon, Nonsense Cholesterol, Dietary Bezafibrate Epichlorohydrin Carrier Proteins DNA Helicases Apolipoproteins A Simvastatin Insulin Pyrroles Fatty Acids, Nonesterified Apolipoprotein E3 DNA Primers Gemfibrozil Apolipoprotein B-48 Lipoproteins, IDL Proteins Membrane Proteins Pravastatin Plant Extracts Chylomicrons Lipase DNA Apolipoprotein A-II Upstream Stimulatory Factors Apolipoprotein B-100

Analytical, Diagnostic and Therapeutic Techniques and Equipment28

Pedigree Risk Factors Disease Models, Animal Genetic Testing Obesity Prevalence Case-Control Studies Prenatal Diagnosis Treatment Outcome DNA Mutational Analysis Chromosome Mapping Diet, Atherogenic Severity of Illness Index Body Weight Retrospective Studies Polymerase Chain Reaction Magnetic Resonance Imaging Heterozygote Detection Cohort Studies Questionnaires Preimplantation Diagnosis Phytotherapy Genetic Therapy Models, Biological Risk Assessment Follow-Up Studies Cross-Sectional Studies Reference Values

Psychiatry and Psychology29

Bipolar Disorder Mental Disorders Anxiety Disorders Mood Disorders Depressive Disorder, Major Autistic Disorder Attention Deficit Disorder with Hyperactivity Depressive Disorder Obsessive-Compulsive Disorder Stress Disorders, Post-Traumatic Phobic Disorders Child Development Disorders, Pervasive Psychotic Disorders Substance-Related Disorders Conduct Disorder Tic Disorders Psychiatric Status Rating Scales Borderline Personality Disorder Somatoform Disorders Cognition Disorders Sleep Disorders Intellectual Disability Huntington Disease Alcohol-Related Disorders Combat Disorders Attention Deficit and Disruptive Behavior Disorders Impulse Control Disorders Schizophrenia Antisocial Personality Disorder

Phenomena and Processes40

Mutation Phenotype Lipid Metabolism Heterozygote Genes, Recessive Genetic Predisposition to Disease Alleles Genetic Linkage Obesity Genotype Base Sequence Point Mutation Homozygote Time Factors Consanguinity Mutation, Missense Diet, Atherogenic Codon, Nonsense Pregnancy Polymorphism, Single Nucleotide Genes, Neurofibromatosis 1 Insulin Resistance Body Weight Haplotypes Gene Expression Regulation Postprandial Period Exons Endophenotypes Amino Acid Sequence Polymorphism, Genetic Signal Transduction Genes, Dominant Lod Score Chromosomes, Human, Pair 22 Chromosome Aberrations Gene Frequency Gene Expression Diet, High-Fat Diet Oxidative Stress

Disciplines and Occupations2

Genetic Counseling Genetics, Medical

Technology, Industry, Agriculture2

Dietary Fats Poloxamer

Humanities1

Information Science6

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

Named Groups1

Infant, Newborn

Health Care19

Risk Factors Genetic Counseling Genetic Testing Genetic Services Comorbidity Prevalence Case-Control Studies Treatment Outcome Family Health Severity of Illness Index Age Factors Retrospective Studies Cohort Studies Questionnaires Sex Factors Risk Assessment Follow-Up Studies Age of Onset Cross-Sectional Studies

Geographicals2

Mediterranean Islands United States

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

Rare Diseases Progeria Myositis Ossificans Hyperlipidemia, Familial Combined Syndrome Mutation Hyperlipidemias Genetic Diseases, Inborn Bipolar Disorder Mental Disorders Triglycerides Anxiety Disorders Hypolipidemic Agents Mood Disorders Lipids Cholesterol Phenotype Pedigree Diagnostic and Statistical Manual of Mental Disorders Hypertriglyceridemia Cholesterol, LDL Williams Syndrome Risk Factors Depressive Disorder, Major Autistic Disorder Bone Diseases, Developmental Disease Models, Animal Musculoskeletal Abnormalities Hyperlipoproteinemia Type IV Lipoproteins Attention Deficit Disorder with Hyperactivity Lipid Metabolism Apolipoproteins E Metabolism, Inborn Errors Hypercholesterolemia Depressive Disorder Apolipoproteins B Liver Cholesterol, HDL Apolipoproteins C Hyperlipoproteinemia Type II Obsessive-Compulsive Disorder Apolipoprotein E2 Stress Disorders, Post-Traumatic Apolipoprotein C-III Mice, Inbred C57BL Heterozygote Genes, Recessive Genetic Counseling Prader-Willi Syndrome Lipoprotein Lipase Xanthomatosis Fenofibrate Lipoproteins, VLDL Phobic Disorders Genetic Predisposition to Disease Genetic Testing Alleles Child Development Disorders, Pervasive Iron Metabolism Disorders Psychotic Disorders Substance-Related Disorders Mice, Knockout Anticholesteremic Agents Molecular Sequence Data Genetic Services Genetic Linkage Mediterranean Islands Arteriosclerosis Ataxia Telangiectasia Neurofibromin 1 Neurofibromatosis 1 Chromosome Disorders Hydroxymethylglutaryl-CoA Reductase Inhibitors Obesity Comorbidity Apolipoproteins Eugenics Lipoproteins, LDL Genotype Base Sequence Cholesterol, VLDL Prevalence Abnormalities, Multiple Pachyonychia Congenita Gynostemma Ectodermal Dysplasia Case-Control Studies Bloom Syndrome Tuberous Sclerosis Point Mutation Homozygote Receptors, LDL Conduct Disorder Dietary Fats Time Factors Prenatal Diagnosis Consanguinity Chondrodysplasia Punctata Treatment Outcome

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