Syndrome abnormalities multiple. Medical search. Frequent questions

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Anatomy10

Brain Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 11 Kidney Face Chromosomes, Human, Pair 21 Cells, Cultured Chromosomes, Human, X

Organisms7

Porcine respiratory and reproductive syndrome virus Mice, Knockout Mice, Inbred C57BL White spot syndrome virus 1 Mice, Mutant Strains Mice, Transgenic SARS Virus

Diseases166

Syndrome Down Syndrome Metabolic Syndrome X Abnormalities, Multiple Nephrotic Syndrome Sjogren's Syndrome Turner Syndrome Myelodysplastic Syndromes Cushing Syndrome Chromosome Aberrations Williams Syndrome Polycystic Ovary Syndrome Acute Coronary Syndrome DiGeorge Syndrome Eye Abnormalities Prader-Willi Syndrome Long QT Syndrome Horner Syndrome Chromosome Disorders Craniofacial Abnormalities Hemolytic-Uremic Syndrome Klinefelter Syndrome Guillain-Barre Syndrome Tourette Syndrome Congenital Abnormalities Antiphospholipid Syndrome Compartment Syndromes Intellectual Disability Porcine Reproductive and Respiratory Syndrome Carpal Tunnel Syndrome Bartter Syndrome Reye Syndrome Werner Syndrome Brugada Syndrome HELLP Syndrome Ehlers-Danlos Syndrome Bloom Syndrome Sturge-Weber Syndrome Job Syndrome Angelman Syndrome Respiratory Distress Syndrome, Adult Wiskott-Aldrich Syndrome Trisomy Restless Legs Syndrome Severe Acute Respiratory Syndrome Disease Models, Animal Paraneoplastic Syndromes Acquired Immunodeficiency Syndrome Skin Abnormalities Facies Cardiovascular Abnormalities Sweet Syndrome Chediak-Higashi Syndrome Urogenital Abnormalities Churg-Strauss Syndrome Musculoskeletal Abnormalities Budd-Chiari Syndrome Chromosome Deletion Kallmann Syndrome Beckwith-Wiedemann Syndrome Wolff-Parkinson-White Syndrome Sezary Syndrome Sick Sinus Syndrome Bardet-Biedl Syndrome Alagille Syndrome Sex Chromosome Aberrations Heart Defects, Congenital Immunologic Deficiency Syndromes Usher Syndromes Stevens-Johnson Syndrome Felty Syndrome Smith-Lemli-Opitz Syndrome Cockayne Syndrome Oculocerebrorenal Syndrome Hand Deformities, Congenital Behcet Syndrome Fetal Diseases Acute Disease Goldenhar Syndrome Orofaciodigital Syndromes ACTH Syndrome, Ectopic Peutz-Jeghers Syndrome Duane Retraction Syndrome Hemorrhagic Fever with Renal Syndrome Hepatopulmonary Syndrome Brain Diseases Translocation, Genetic Limb Deformities, Congenital Stiff-Person Syndrome Proteus Syndrome Short Bowel Syndrome Microcephaly Zollinger-Ellison Syndrome Serotonin Syndrome Klippel-Feil Syndrome Mobius Syndrome Complex Regional Pain Syndromes Respiratory Distress Syndrome, Newborn Thoracic Outlet Syndrome Neurocutaneous Syndromes Neoplastic Syndromes, Hereditary Hermanski-Pudlak Syndrome Aneuploidy LEOPARD Syndrome Dwarfism Nervous System Malformations Syndactyly Sleep Apnea Syndromes Insulin Resistance Neuroleptic Malignant Syndrome Costello Syndrome Subclavian Steal Syndrome Hantavirus Pulmonary Syndrome Waardenburg Syndrome Obesity Polyradiculoneuropathy Adie Syndrome Growth Disorders Wolfram Syndrome Agenesis of Corpus Callosum Systemic Inflammatory Response Syndrome Li-Fraumeni Syndrome Foot Deformities, Congenital Hamartoma Syndrome, Multiple Rubinstein-Taybi Syndrome Pigmentation Disorders Hepatorenal Syndrome Nervous System Diseases Sudden Infant Death Gitelman Syndrome Tooth Abnormalities Coloboma Hypertelorism Muscle Hypotonia Ovarian Hyperstimulation Syndrome Genetic Predisposition to Disease Abnormalities, Drug-Induced Ectodermal Dysplasia Premenstrual Syndrome Miller Fisher Syndrome Capillary Leak Syndrome Korsakoff Syndrome Poland Syndrome Rothmund-Thomson Syndrome Craniosynostoses Alstrom Syndrome Disease Progression Acquired Hyperostosis Syndrome Recurrence Acrocephalosyndactylia CREST Syndrome Wasting Syndrome Ocular Motility Disorders Superior Vena Cava Syndrome Hypoplastic Left Heart Syndrome Mouth Abnormalities Smith-Magenis Syndrome Micrognathism Myasthenic Syndromes, Congenital Zellweger Syndrome Chronic Disease Bone Diseases, Developmental Progeria Heterotaxy Syndrome Malabsorption Syndromes Hearing Loss, Sensorineural

Chemicals and Drugs4

Biological Markers Wiskott-Aldrich Syndrome Protein Blood Glucose Autoantibodies

Analytical, Diagnostic and Therapeutic Techniques and Equipment40

Karyotyping Pedigree Magnetic Resonance Imaging Risk Factors Retrospective Studies Case-Control Studies Treatment Outcome Disease Models, Animal Prospective Studies Facies Electrocardiography Follow-Up Studies In Situ Hybridization, Fluorescence DNA Mutational Analysis Tomography, X-Ray Computed Prevalence Prenatal Diagnosis Fatal Outcome Prognosis Severity of Illness Index Sensitivity and Specificity Cohort Studies Predictive Value of Tests Biopsy Ultrasonography, Prenatal Chromosome Banding Reference Values Polymerase Chain Reaction Obesity Chromosome Mapping Genetic Testing Cytogenetic Analysis Analysis of Variance Incidence Cross-Sectional Studies Echocardiography Immunohistochemistry Risk Assessment Neurologic Examination Electroencephalography

Psychiatry and Psychology8

Tourette Syndrome Intellectual Disability Restless Legs Syndrome Asperger Syndrome Schizophrenia Developmental Disabilities Korsakoff Syndrome Munchausen Syndrome

Phenomena and Processes34

Chromosome Aberrations Mutation Phenotype Pregnancy Trisomy Time Factors Chromosome Deletion Sex Chromosome Aberrations Heterozygote Homozygote Mutation, Missense Base Sequence Translocation, Genetic Mosaicism Chromosomes, Human, Pair 22 Consanguinity Sensitivity and Specificity Genotype Genes, Recessive Aneuploidy Insulin Resistance Obesity Gene Deletion Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 15 Genetic Predisposition to Disease Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 21 Alleles Genetic Linkage Amino Acid Sequence Gestational Age Chromosomes, Human, X Exons

Disciplines and Occupations2

Immunohistochemistry Cytogenetics

Information Science7

Prevalence Molecular Sequence Data Fatal Outcome Base Sequence Incidence Amino Acid Sequence Image Processing, Computer-Assisted

Named Groups1

Infant, Newborn

Health Care18

Risk Factors Retrospective Studies Case-Control Studies Treatment Outcome Prospective Studies Follow-Up Studies Prevalence Fatal Outcome Severity of Illness Index Sensitivity and Specificity Cohort Studies Predictive Value of Tests Age Factors Genetic Testing Analysis of Variance Incidence Cross-Sectional Studies Risk Assessment

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

Syndrome Down Syndrome Metabolic Syndrome X Abnormalities, Multiple Nephrotic Syndrome Sjogren's Syndrome Turner Syndrome Myelodysplastic Syndromes Cushing Syndrome Chromosome Aberrations Williams Syndrome Polycystic Ovary Syndrome Acute Coronary Syndrome DiGeorge Syndrome Eye Abnormalities Prader-Willi Syndrome Mutation Long QT Syndrome Horner Syndrome Phenotype Chromosome Disorders Karyotyping Pedigree Magnetic Resonance Imaging Craniofacial Abnormalities Hemolytic-Uremic Syndrome Klinefelter Syndrome Guillain-Barre Syndrome Tourette Syndrome Congenital Abnormalities Antiphospholipid Syndrome Compartment Syndromes Intellectual Disability Porcine Reproductive and Respiratory Syndrome Carpal Tunnel Syndrome Bartter Syndrome Pregnancy Reye Syndrome Werner Syndrome Brugada Syndrome Infant, Newborn HELLP Syndrome Ehlers-Danlos Syndrome Porcine respiratory and reproductive syndrome virus Bloom Syndrome Risk Factors Sturge-Weber Syndrome Job Syndrome Brain Angelman Syndrome Respiratory Distress Syndrome, Adult Retrospective Studies Wiskott-Aldrich Syndrome Case-Control Studies Trisomy Treatment Outcome Restless Legs Syndrome Severe Acute Respiratory Syndrome Disease Models, Animal Time Factors Paraneoplastic Syndromes Acquired Immunodeficiency Syndrome Prospective Studies Skin Abnormalities Facies Cardiovascular Abnormalities Electrocardiography Follow-Up Studies Sweet Syndrome Chediak-Higashi Syndrome Urogenital Abnormalities Churg-Strauss Syndrome Musculoskeletal Abnormalities Budd-Chiari Syndrome In Situ Hybridization, Fluorescence DNA Mutational Analysis Chromosome Deletion Kallmann Syndrome Tomography, X-Ray Computed Beckwith-Wiedemann Syndrome Wolff-Parkinson-White Syndrome Sezary Syndrome Sick Sinus Syndrome Prevalence Bardet-Biedl Syndrome Alagille Syndrome Molecular Sequence Data Sex Chromosome Aberrations Prenatal Diagnosis Heterozygote Heart Defects, Congenital Immunologic Deficiency Syndromes Usher Syndromes Fatal Outcome Stevens-Johnson Syndrome Felty Syndrome Smith-Lemli-Opitz Syndrome Prognosis Cockayne Syndrome Severity of Illness Index

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