Clinical phenotype of asthma. Medical search. Frequent questions

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Anatomy17

Cells, Cultured Lung Chromosomes, Human, X Eosinophils Bronchi Fibroblasts Cell Line X Chromosome Brain Chromosomes, Human, Pair 5 Sputum Chromosomes, Human, Pair 15 Th2 Cells Chromosomes, Human, Pair 4 Skin Respiratory System Chromosomes, Human, Pair 7

Organisms7

Mice, Inbred C57BL Mice, Knockout Mice, Transgenic Pyroglyphidae Mites Mice, Inbred BALB C Mice, Mutant Strains

Diseases79

Asthma Syndrome Asthma, Exercise-Induced Genetic Predisposition to Disease Asthma, Occupational Bronchial Hyperreactivity Respiratory Sounds Abnormalities, Multiple Hypersensitivity Mitochondrial Diseases Hypersensitivity, Immediate Intellectual Disability Disease Models, Animal Rhinitis Mucopolysaccharidosis VI Rhinitis, Allergic, Perennial Myotonic Disorders Chromosome Deletion Disease Progression Genetic Diseases, Inborn Muscular Dystrophies, Limb-Girdle Airway Remodeling MELAS Syndrome Status Asthmaticus Common Variable Immunodeficiency Genetic Diseases, X-Linked Mitochondrial Encephalomyopathies Bronchitis Mental Retardation, X-Linked Long QT Syndrome Muscular Dystrophies Respiratory Hypersensitivity Craniofacial Abnormalities Panuveitis Ophthalmia, Sympathetic Distal Myopathies Microcephaly Retinoschisis Muscle Hypotonia Pulmonary Disease, Chronic Obstructive Muscular Diseases Ophthalmoplegia, Chronic Progressive External Hereditary Sensory and Motor Neuropathy Marfan Syndrome Mitochondrial Myopathies Chronic Disease Asthma, Aspirin-Induced Renal Tubular Transport, Inborn Errors alpha-Thalassemia Frontotemporal Dementia Amino Acid Metabolism, Inborn Errors beta-Thalassemia Charcot-Marie-Tooth Disease Airway Obstruction Supranuclear Palsy, Progressive Eosinophilia Ataxia Fragile X Syndrome Cough Uniparental Disomy Peroxisomal Disorders Congenital Disorders of Glycosylation Cardiomyopathy, Hypertrophic Occupational Diseases Mucopolysaccharidosis III Paralyses, Familial Periodic Chondrodysplasia Punctata Leber Congenital Amaurosis Myopathies, Nemaline Frontotemporal Lobar Degeneration Homocystinuria Leigh Disease Retinitis Pigmentosa Arthrogryposis Monosomy Angelman Syndrome Inflammation Thalassemia Carbohydrate Metabolism, Inborn Errors

Chemicals and Drugs41

Anti-Asthmatic Agents Bronchodilator Agents Allergens Adrenal Cortex Hormones Codon, Nonsense Chondro-4-Sulfatase Albuterol Methacholine Chloride Budesonide Beclomethasone Leukotriene Antagonists RNA, Messenger DNA, Mitochondrial Membrane Proteins NAV1.5 Voltage-Gated Sodium Channel Genetic Markers Bronchoconstrictor Agents Hemoglobin E Ovalbumin Hemoglobin H Adrenergic beta-Agonists Biological Markers Transcription Factors DNA Primers DNA-Binding Proteins Carrier Proteins RNA Splice Sites DNA Proteins Cytokines Glucocorticoids Eye Proteins Anti-Inflammatory Agents Nuclear Proteins Air Pollutants Homeodomain Proteins Autoantibodies Interleukin-13 Hemoglobins, Abnormal Nedocromil Androstadienes

Analytical, Diagnostic and Therapeutic Techniques and Equipment50

Pedigree DNA Mutational Analysis Administration, Inhalation Peak Expiratory Flow Rate Forced Expiratory Volume Respiratory Sounds Genetic Association Studies Severity of Illness Index Polymerase Chain Reaction Cohort Studies Chromosome Mapping Respiratory Function Tests Genetic Testing Disease Models, Animal Case-Control Studies Prevalence Spirometry Risk Factors Sequence Analysis, DNA Amino Acid Substitution Heterozygote Detection Nebulizers and Vaporizers Skin Tests Gene Expression Profiling Reverse Transcriptase Polymerase Chain Reaction Genetic Complementation Test Questionnaires Immunohistochemistry Cross-Sectional Studies Models, Genetic Genome-Wide Association Study Oligonucleotide Array Sequence Analysis Blotting, Western Vital Capacity Treatment Outcome Bronchoalveolar Lavage Fluid Cloning, Molecular Retrospective Studies Cluster Analysis Transfection In Situ Hybridization, Fluorescence Follow-Up Studies Breath Tests Mutagenesis, Insertional Models, Biological Prospective Studies Prognosis Karyotyping Airway Resistance Magnetic Resonance Imaging

Psychiatry and Psychology6

Intellectual Disability Frontotemporal Dementia Siblings Family Frontotemporal Lobar Degeneration Developmental Disabilities

Phenomena and Processes67

Phenotype Mutation Genotype Mutation, Missense Genetic Predisposition to Disease Alleles Homozygote Heterozygote Peak Expiratory Flow Rate Forced Expiratory Volume Base Sequence Respiratory Sounds Point Mutation Genetic Heterogeneity Genetic Linkage Exons Penetrance Codon, Nonsense Polymorphism, Single Nucleotide Polymorphism, Genetic Frameshift Mutation Gene Deletion Genes, Dominant Amino Acid Sequence Consanguinity Haplotypes Genetic Variation Genes, Recessive Sequence Deletion Chromosomes, Human, X Amino Acid Substitution Chromosome Deletion Gene Frequency Polymorphism, Single-Stranded Conformational Airway Remodeling Genetic Markers DNA Repeat Expansion Gene Expression Bronchoconstriction Time Factors Signal Transduction X Chromosome Gene Expression Regulation RNA Splice Sites Chromosomes, Human, Pair 5 Vital Capacity Gene Dosage Microsatellite Repeats Cell Differentiation Chromosomes, Human, Pair 15 Exhalation Polymorphism, Restriction Fragment Length Transfection Founder Effect Uniparental Disomy Lod Score Chromosomes, Human, Pair 4 Genome, Human Mutagenesis, Insertional Sequence Homology, Amino Acid Genetic Loci Genes, X-Linked Monosomy Linkage Disequilibrium Chromosomes, Human, Pair 7 Airway Resistance Protein Structure, Tertiary

Disciplines and Occupations2

Immunohistochemistry Pulmonary Medicine

Anthropology, Education, Sociology and Social Phenomena2

Siblings Family

Information Science5

Molecular Sequence Data Base Sequence Amino Acid Sequence Prevalence Questionnaires

Named Groups3

Infant, Newborn Asian Continental Ancestry Group Siblings

Health Care19

Age of Onset Severity of Illness Index Family Health Cohort Studies Genetic Testing Case-Control Studies Prevalence Risk Factors Questionnaires Cross-Sectional Studies Genome-Wide Association Study Treatment Outcome Retrospective Studies Cluster Analysis Environmental Exposure Air Pollution, Indoor Age Factors Follow-Up Studies Prospective Studies

Geographicals2

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 Information Science Named Groups Health Care Geographicals

Asthma Phenotype Mutation Pedigree Anti-Asthmatic Agents DNA Mutational Analysis Genotype Mutation, Missense Syndrome Asthma, Exercise-Induced Age of Onset Molecular Sequence Data Administration, Inhalation Genetic Predisposition to Disease Alleles Homozygote Heterozygote Peak Expiratory Flow Rate Asthma, Occupational Forced Expiratory Volume Base Sequence Bronchial Hyperreactivity Respiratory Sounds Bronchodilator Agents Genetic Association Studies Severity of Illness Index Allergens Point Mutation Genetic Heterogeneity Adrenal Cortex Hormones Abnormalities, Multiple Hypersensitivity Family Health Genetic Linkage Exons Penetrance Mitochondrial Diseases Codon, Nonsense Polymorphism, Single Nucleotide Polymorphism, Genetic Polymerase Chain Reaction Frameshift Mutation Hypersensitivity, Immediate Intellectual Disability Cohort Studies Gene Deletion Chromosome Mapping Genes, Dominant Amino Acid Sequence Consanguinity Respiratory Function Tests Genetic Testing Haplotypes Disease Models, Animal Case-Control Studies Rhinitis Chondro-4-Sulfatase Prevalence Mucopolysaccharidosis VI Albuterol Methacholine Chloride Genetic Variation Genes, Recessive Rhinitis, Allergic, Perennial Cells, Cultured Infant, Newborn Sequence Deletion Lung Chromosomes, Human, X Spirometry Risk Factors Sequence Analysis, DNA Eosinophils Bronchi Budesonide Myotonic Disorders Amino Acid Substitution Heterozygote Detection Beclomethasone Leukotriene Antagonists Chromosome Deletion Disease Progression Gene Frequency RNA, Messenger Genetic Diseases, Inborn Fibroblasts Muscular Dystrophies, Limb-Girdle Nebulizers and Vaporizers Skin Tests Mice, Inbred C57BL Polymorphism, Single-Stranded Conformational DNA, Mitochondrial Membrane Proteins Mice, Knockout Airway Remodeling NAV1.5 Voltage-Gated Sodium Channel Genetic Markers Bronchoconstrictor Agents Cell Line Gene Expression Profiling

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