Genetic defect disorder. Medical search. Frequent questions

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Anatomy19

Cells, Cultured Fibroblasts Brain Cell Line Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 10 Skin Chromosomes, Human, Pair 1 Lysosomes Chromosomes, Human, Pair 4 Hybrid Cells Chromosomes, Human, Pair 15 Liver X Chromosome Neurons Chromosomes, Human, Pair 2 B-Lymphocytes Mitochondria Chromosomes, Human, Pair 17

Organisms8

Mice, Mutant Strains Mice, Knockout Mice, Inbred C57BL Mice, Transgenic Rats, Mutant Strains Zebrafish Mice, Inbred Strains Cricetinae

Diseases71

Metabolism, Inborn Errors Syndrome Mitochondrial Diseases Glycogen Storage Disease Type VII Substance-Related Disorders Heart Septal Defects, Ventricular Heart Defects, Congenital Genetic Diseases, Inborn Mitochondrial Encephalomyopathies Disease Models, Animal Heart Septal Defects, Atrial Genetic Predisposition to Disease Lymphoproliferative Disorders Carbohydrate Metabolism, Inborn Errors Protein C Deficiency Lipid Metabolism, Inborn Errors Tic Disorders Immunologic Deficiency Syndromes Autoimmune Lymphoproliferative Syndrome Cataract Chediak-Higashi Syndrome Dwarfism Afibrinogenemia Sleep Disorders Factor XIII Deficiency Lymphohistiocytosis, Hemophagocytic Intellectual Disability Granulomatous Disease, Chronic Amino Acid Metabolism, Inborn Errors Congenital Hypothyroidism Heart Septal Defects Hand Deformities, Congenital Bernard-Soulier Syndrome Facies Factor V Deficiency Movement Disorders Common Variable Immunodeficiency Microphthalmos Muscular Dystrophies Alcohol-Related Disorders Severe Combined Immunodeficiency Speech Disorders Menkes Kinky Hair Syndrome Crigler-Najjar Syndrome Genetic Diseases, X-Linked Thrombasthenia Purine-Pyrimidine Metabolism, Inborn Errors Agammaglobulinemia Protein S Deficiency Infertility, Male Myeloproliferative Disorders Abnormalities, Multiple Chromosome Deletion Temporomandibular Joint Disorders Autoimmune Diseases Lecithin Acyltransferase Deficiency Retinitis Pigmentosa Congenital Abnormalities Learning Disorders Retinal Degeneration Nervous System Diseases Neoplastic Syndromes, Hereditary Chromosome Aberrations Muscular Dystrophy, Duchenne Peroxisomal Disorders Congenital Disorders of Glycosylation Blood Platelet Disorders Alcoholism Fetal Alcohol Spectrum Disorders Hemorrhagic Disorders Disease Progression

Chemicals and Drugs26

Codon, Nonsense RNA, Messenger Sarcoglycans beta-Crystallin A Chain DNA DNA-Binding Proteins Membrane Proteins Genetic Markers DNA Primers Transcription Factors gamma-Crystallins Carrier Proteins DNA, Mitochondrial beta-Crystallin B Chain Proteins Nuclear Proteins Eye Proteins RNA Splice Sites Codon, Terminator Antimanic Agents Factor V Dystrophin Connexins Apolipoproteins C Membrane Glycoproteins Cytoskeletal Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment34

Pedigree DNA Mutational Analysis Chromosome Mapping Disease Models, Animal Polymerase Chain Reaction Heterozygote Detection Case-Control Studies Genetic Testing Facies Genetic Complementation Test Risk Factors Sequence Analysis, DNA Magnetic Resonance Imaging Models, Biological Amino Acid Substitution Prevalence Genetic Therapy Reference Values Transfection Cloning, Molecular Severity of Illness Index Immunohistochemistry Crosses, Genetic Sequence Alignment Treatment Outcome Blotting, Western Questionnaires Cohort Studies Electroretinography Models, Genetic Reverse Transcriptase Polymerase Chain Reaction Blotting, Southern Diagnosis, Dual (Psychiatry)Follow-Up Studies

Psychiatry and Psychology43

Bipolar Disorder Mental Disorders Anxiety Disorders Mood Disorders Depressive Disorder, Major Attention Deficit Disorder with Hyperactivity Depressive Disorder Obsessive-Compulsive Disorder Autistic 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 Alcohol-Related Disorders Combat Disorders Attention Deficit and Disruptive Behavior Disorders Impulse Control Disorders Schizophrenia Antisocial Personality Disorder Binge-Eating Disorder Dysthymic Disorder Interview, Psychological Dissociative Disorders Learning Disorders Conversion Disorder Schizotypal Personality Disorder Neurotic Disorders Siblings Nuclear Family Affective Disorders, Psychotic Alcoholism Personality Assessment Body Dysmorphic Disorders Adjustment Disorders

Phenomena and Processes67

Mutation Phenotype Consanguinity Base Sequence Homozygote Genes, Recessive Genetic Linkage Mutation, Missense Heterozygote Genes, Dominant Exons Codon, Nonsense Amino Acid Sequence Point Mutation Genotype Frameshift Mutation Genetic Predisposition to Disease Gene Deletion Alleles Lod Score Sequence Deletion Genetic Heterogeneity Pregnancy Signal Transduction Haplotypes Genetic Markers Introns Time Factors Exome Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 10 Polymorphism, Single-Stranded Conformational Amino Acid Substitution Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 4 Polymorphism, Restriction Fragment Length Polymorphism, Genetic Gene Expression RNA Splicing Transfection Gene Expression Regulation Chromosome Deletion Sequence Homology, Amino Acid Chromosomes, Human, Pair 15 Cell Differentiation X Chromosome DNA Repair Genes Genetic Vectors Chromosomes, Human, Pair 2 Recombination, Genetic RNA Splice Sites Chromosome Aberrations Codon, Terminator Apoptosis Polymorphism, Single Nucleotide Microsatellite Repeats Protein Transport Protein Structure, Tertiary Mutagenesis Germ-Line Mutation Transgenes Chromosomes, Human, Pair 17 Glycosylation Gene Expression Regulation, Developmental Aging DNA Damage

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena2

Siblings Nuclear Family

Information Science6

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

Named Groups3

Infant, Newborn Asian Continental Ancestry Group Siblings

Health Care13

Age of Onset Family Health Case-Control Studies Comorbidity Genetic Testing Risk Factors Prevalence Severity of Illness Index Age Factors Treatment Outcome Questionnaires Cohort Studies Follow-Up Studies

Geographicals1

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

Mutation Bipolar Disorder Pedigree Mental Disorders Anxiety Disorders Mood Disorders Phenotype Diagnostic and Statistical Manual of Mental Disorders Molecular Sequence Data Consanguinity DNA Mutational Analysis Metabolism, Inborn Errors Base Sequence Syndrome Homozygote Genes, Recessive Genetic Linkage Depressive Disorder, Major Mutation, Missense Attention Deficit Disorder with Hyperactivity Heterozygote Mitochondrial Diseases Genes, Dominant Depressive Disorder Exons Glycogen Storage Disease Type VII Obsessive-Compulsive Disorder Autistic Disorder Stress Disorders, Post-Traumatic Codon, Nonsense Chromosome Mapping Phobic Disorders Amino Acid Sequence Child Development Disorders, Pervasive Psychotic Disorders Substance-Related Disorders Heart Septal Defects, Ventricular Heart Defects, Congenital Point Mutation Genetic Diseases, Inborn Genotype Mitochondrial Encephalomyopathies Frameshift Mutation Disease Models, Animal Heart Septal Defects, Atrial Genetic Predisposition to Disease Lymphoproliferative Disorders Carbohydrate Metabolism, Inborn Errors Polymerase Chain Reaction Gene Deletion Protein C Deficiency Conduct Disorder Lipid Metabolism, Inborn Errors Mice, Mutant Strains Alleles Tic Disorders Immunologic Deficiency Syndromes Autoimmune Lymphoproliferative Syndrome Mice, Knockout Cells, Cultured Cataract Psychiatric Status Rating Scales Lod Score Fibroblasts Chediak-Higashi Syndrome Age of Onset Infant, Newborn Dwarfism RNA, Messenger Borderline Personality Disorder Brain Mice, Inbred C57BL Afibrinogenemia Somatoform Disorders Cognition Disorders Sequence Deletion Sleep Disorders Sarcoglycans Factor XIII Deficiency Heterozygote Detection Lymphohistiocytosis, Hemophagocytic Genetic Heterogeneity Pregnancy Family Health Intellectual Disability Signal Transduction Granulomatous Disease, Chronic Amino Acid Metabolism, Inborn Errors beta-Crystallin A Chain DNA Case-Control Studies Haplotypes Congenital Hypothyroidism DNA-Binding Proteins Heart Septal Defects Comorbidity Genetic Testing Hand Deformities, Congenital Bernard-Soulier Syndrome Membrane Proteins

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