Syndrome immune genetic diseases x linked. Medical search. Frequent questions

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Anatomy21

Immune System X Chromosome T-Lymphocytes Cells, Cultured Immune Sera Cell Line Spleen Lymphocytes Dendritic Cells CD4-Positive T-Lymphocytes Macrophages B-Lymphocytes Liver Skin Chromosomes, Human Fibroblasts Brain Killer Cells, Natural Th1 Cells T-Lymphocytes, Regulatory Lung

Organisms7

Mice, Inbred C57BL Mice, Knockout Mice, Inbred BALB C Porcine respiratory and reproductive syndrome virus Mice, Transgenic Mice, Mutant Strains Dependovirus

Diseases99

Genetic Diseases, Inborn Syndrome Down Syndrome Metabolic Syndrome X Nephrotic Syndrome Sjogren's Syndrome Abnormalities, Multiple Disease Models, Animal Genetic Diseases, Y-Linked Turner Syndrome Rare Diseases Genetic Diseases, X-Linked Myelodysplastic Syndromes Genetic Predisposition to Disease Cushing Syndrome Disease Cystic Fibrosis Acute Coronary Syndrome Polycystic Ovary Syndrome Williams Syndrome DiGeorge Syndrome Metabolism, Inborn Errors Horner Syndrome Prader-Willi Syndrome Long QT Syndrome Intellectual Disability Guillain-Barre Syndrome Immune System Diseases Kallmann Syndrome Hemolytic-Uremic Syndrome Immune Complex Diseases Porcine Reproductive and Respiratory Syndrome Tourette Syndrome Compartment Syndromes Chromosome Disorders Antiphospholipid Syndrome Klinefelter Syndrome Acquired Immunodeficiency Syndrome Carpal Tunnel Syndrome Werner Syndrome Reye Syndrome Bartter Syndrome HELLP Syndrome Neoplasms Fanconi Anemia Bloom Syndrome Brugada Syndrome Sphingolipidoses Ehlers-Danlos Syndrome Respiratory Distress Syndrome, Adult Chromosome Aberrations Severe Acute Respiratory Syndrome Angelman Syndrome Wiskott-Aldrich Syndrome Immunologic Deficiency Syndromes Job Syndrome Inflammation Restless Legs Syndrome Paraneoplastic Syndromes Sweet Syndrome Tuberous Sclerosis Mucopolysaccharidosis I Immune Reconstitution Inflammatory Syndrome Tay-Sachs Disease Muscular Dystrophy, Duchenne Kartagener Syndrome Churg-Strauss Syndrome Sturge-Weber Syndrome Autoimmune Diseases Chediak-Higashi Syndrome Budd-Chiari Syndrome Congenital Abnormalities Hemophilia B beta-Thalassemia Felty Syndrome Hemochromatosis Lipid Metabolism Disorders Wolff-Parkinson-White Syndrome Homocystinuria Facies Dysautonomia, Familial Sezary Syndrome Stevens-Johnson Syndrome Hemophilia A Sick Sinus Syndrome Polycystic Kidney Diseases Mitochondrial Diseases Usher Syndromes Muscular Dystrophies Phenylketonurias Beckwith-Wiedemann Syndrome Hemorrhagic Fever with Renal Syndrome Behcet Syndrome Alagille Syndrome alpha 1-Antitrypsin Deficiency Bardet-Biedl Syndrome ACTH Syndrome, Ectopic Ataxia Telangiectasia Peutz-Jeghers Syndrome

Chemicals and Drugs28

Codon, Nonsense Antigen-Antibody Complex Cystic Fibrosis Transmembrane Conductance Regulator Immune Sera Immunoglobulin G Cytokines DNA RNA, Messenger Interferon-gamma Genetic Markers Membrane Proteins Proteins Antibodies, Viral Factor IX Adjuvants, Immunologic DNA Primers Recombinant Proteins DNA-Binding Proteins Immunoglobulin M Autoantibodies Dystrophin Antigens Biological Markers Wiskott-Aldrich Syndrome Protein Carrier Proteins Transcription Factors Immunoglobulin A Steroid 21-Hydroxylase

Analytical, Diagnostic and Therapeutic Techniques and Equipment34

Disease Models, Animal Pedigree Genetic Testing Genetic Therapy Chromosome Mapping Prenatal Diagnosis DNA Mutational Analysis Models, Genetic Polymerase Chain Reaction Lymphocyte Activation Heterozygote Detection Models, Biological Flow Cytometry Gene Transfer Techniques Sequence Analysis, DNA Risk Factors Targeted Gene Repair Case-Control Studies Genetic Techniques Enzyme-Linked Immunosorbent Assay Gene Expression Profiling Preimplantation Diagnosis Karyotyping Immunization Treatment Outcome Oligonucleotide Array Sequence Analysis Gene Targeting Facies Models, Immunological Genetic Association Studies Transfection Immunohistochemistry In Situ Hybridization, Fluorescence Cohort Studies

Psychiatry and Psychology3

Intellectual Disability Tourette Syndrome Restless Legs Syndrome

Phenomena and Processes62

Mutation Phenotype Immune Tolerance Base Sequence Immunity, Innate X Chromosome Genome, Human Genetic Predisposition to Disease Immune Evasion Genotype Codon, Nonsense Genes, Recessive Alleles Immunity, Cellular Pregnancy Amino Acid Sequence Genetic Vectors Immunity Time Factors Lymphocyte Activation Signal Transduction Mutation, Missense Genetic Linkage Heterozygote Antibody Formation Polymorphism, Single Nucleotide Exons Gene Expression Regulation Nonsense Mediated mRNA Decay Genetic Variation Consanguinity Gene Expression Genetic Markers Point Mutation Homozygote Chromosome Aberrations Adaptive Immunity Genes, Dominant Exome Gene Deletion Trinucleotide Repeats Gene Frequency Haploinsufficiency Immunity, Humoral Polymorphism, Genetic Mosaicism Haplotypes Protein Binding Chromosomes, Human Penetrance Protein Structure, Tertiary Immune System Processes Cell Differentiation Sequence Deletion Germ-Line Mutation Recombination, Genetic Evolution, Molecular Transfection Algorithms Genome Alu Elements DNA Repair

Disciplines and Occupations6

Genetics, Medical Genetic Counseling Molecular Biology Human Genome Project Computational Biology Immunohistochemistry

Humanities2

Eugenics Judaism

Information Science7

Molecular Sequence Data Base Sequence Amino Acid Sequence Probability Theory Human Genome Project Databases, Genetic Algorithms

Named Groups1

Infant, Newborn

Health Care7

Genetic Testing Genetic Counseling Risk Factors Case-Control Studies Immunization Treatment Outcome Cohort Studies

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

Genetic Diseases, Inborn Syndrome Immune System Down Syndrome Metabolic Syndrome X Mutation Nephrotic Syndrome Sjogren's Syndrome Phenotype Immune Tolerance Eugenics Genetics, Medical Abnormalities, Multiple Molecular Sequence Data Disease Models, Animal Genetic Diseases, Y-Linked Pedigree Turner Syndrome Mice, Inbred C57BL Base Sequence Immunity, Innate Rare Diseases Genetic Testing X Chromosome Genetic Diseases, X-Linked Myelodysplastic Syndromes Genome, Human Genetic Counseling Genetic Predisposition to Disease Cushing Syndrome Genetic Therapy Disease Chromosome Mapping Prenatal Diagnosis Cystic Fibrosis DNA Mutational Analysis Immune Evasion Genotype Codon, Nonsense Acute Coronary Syndrome T-Lymphocytes Polycystic Ovary Syndrome Antigen-Antibody Complex Models, Genetic Genes, Recessive Cystic Fibrosis Transmembrane Conductance Regulator Alleles Cells, Cultured Immune Sera Polymerase Chain Reaction Williams Syndrome Immunity, Cellular Cell Line Mice, Knockout Immunoglobulin G DiGeorge Syndrome Cytokines Pregnancy Metabolism, Inborn Errors Horner Syndrome Mice, Inbred BALB C Prader-Willi Syndrome Long QT Syndrome Intellectual Disability Judaism Amino Acid Sequence DNA Genetic Vectors Guillain-Barre Syndrome Immune System Diseases Kallmann Syndrome Immunity Time Factors Lymphocyte Activation Signal Transduction Hemolytic-Uremic Syndrome Mutation, Missense Immune Complex Diseases Genetic Linkage Heterozygote Antibody Formation Porcine Reproductive and Respiratory Syndrome Tourette Syndrome Compartment Syndromes Chromosome Disorders Infant, Newborn Antiphospholipid Syndrome Polymorphism, Single Nucleotide Spleen Exons Gene Expression Regulation Porcine respiratory and reproductive syndrome virus Lymphocytes Klinefelter Syndrome Mice, Transgenic Acquired Immunodeficiency Syndrome Carpal Tunnel Syndrome Werner Syndrome Molecular Biology RNA, Messenger

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