Trisomy 13 syndrome. Medical search. Frequent questions

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Anatomy21

Chromosomes, Human, Pair 18 Chromosomes, Human, 16-18 Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 13 Chromosomes, Human, 13-15 Chromosomes, Human, 6-12 and X Chromosomes, Human, 21-22 and Y Nasal Bone Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 12 Neck Chromosomes, Human, 4-5 Chromosomes, Human, 19-20 Chromosomes, Human, 1-3 Fetus Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 11 Forehead Chromosomes, Human, Pair 15

Organisms1

Porcine respiratory and reproductive syndrome virus

Diseases43

Trisomy Syndrome Down Syndrome Abnormalities, Multiple Chromosome Disorders Metabolic Syndrome X Chromosome Aberrations Nondisjunction, Genetic Fetal Diseases Turner Syndrome Nephrotic Syndrome Aneuploidy Sjogren's Syndrome Myelodysplastic Syndromes Intellectual Disability Translocation, Genetic Monosomy Prader-Willi Syndrome Cushing Syndrome Acute Coronary Syndrome Polycystic Ovary Syndrome Williams Syndrome DiGeorge Syndrome Klinefelter Syndrome Horner Syndrome Long QT Syndrome Craniofacial Abnormalities Guillain-Barre Syndrome Hemolytic-Uremic Syndrome Sex Chromosome Aberrations Compartment Syndromes Tourette Syndrome Antiphospholipid Syndrome Heart Defects, Congenital Chromosome Deletion Porcine Reproductive and Respiratory Syndrome Carpal Tunnel Syndrome Werner Syndrome Reye Syndrome Bartter Syndrome Microcephaly Facies HELLP Syndrome

Chemicals and Drugs2

Chorionic Gonadotropin, beta Subunit, Human Pregnancy-Associated Plasma Protein-A

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

Karyotyping Prenatal Diagnosis Nuchal Translucency Measurement Ultrasonography, Prenatal Chromosome Banding Dermatoglyphics Amniocentesis In Situ Hybridization, Fluorescence Crown-Rump Length Chorionic Villi Sampling Pedigree Cytogenetic Analysis Abortion, Eugenic Facies Retrospective Studies

Psychiatry and Psychology2

Intellectual Disability Tourette Syndrome

Phenomena and Processes35

Trisomy Chromosomes, Human, Pair 18 Chromosomes, Human, 16-18 Chromosomes, Human, Pair 21 Mosaicism Chromosomes, Human, Pair 13 Chromosome Aberrations Chromosomes, Human, 13-15 Nondisjunction, Genetic Chromosomes, Human, 6-12 and X Pregnancy Trimester, First Pregnancy Maternal Age Pregnancy Trimester, Second Chromosomes, Human, 21-22 and Y Aneuploidy Pregnancy, High-Risk Translocation, Genetic Crown-Rump Length Monosomy Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 12 Chromosomes, Human, 4-5 Chromosomes, Human, 19-20 Gestational Age Phenotype Chromosomes, Human, 1-3 Sex Chromosome Aberrations Chromosome Deletion Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 11 Mutation Chromosomes, Human, Pair 15

Disciplines and Occupations1

Anthropology, Education, Sociology and Social Phenomena1

Dermatoglyphics

Named Groups1

Infant, Newborn

Health Care3

Maternal Age Crown-Rump Length Retrospective Studies

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 Named Groups Health Care

Trisomy Syndrome Down Syndrome Karyotyping Chromosomes, Human, Pair 18 Abnormalities, Multiple Chromosome Disorders Chromosomes, Human, 16-18 Chromosomes, Human, Pair 21 Prenatal Diagnosis Mosaicism Chromosomes, Human, Pair 13 Metabolic Syndrome X Nuchal Translucency Measurement Chromosome Aberrations Chorionic Gonadotropin, beta Subunit, Human Chromosomes, Human, 13-15 Nondisjunction, Genetic Chromosomes, Human, 6-12 and X Pregnancy Trimester, First Ultrasonography, Prenatal Pregnancy Maternal Age Fetal Diseases Turner Syndrome Pregnancy Trimester, Second Pregnancy-Associated Plasma Protein-A Chromosomes, Human, 21-22 and Y Nasal Bone Nephrotic Syndrome Chromosome Banding Aneuploidy Sjogren's Syndrome Myelodysplastic Syndromes Dermatoglyphics Amniocentesis In Situ Hybridization, Fluorescence Pregnancy, High-Risk Intellectual Disability Translocation, Genetic Crown-Rump Length Monosomy Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 12 Chorionic Villi Sampling Neck Chromosomes, Human, 4-5 Infant, Newborn Chromosomes, Human, 19-20 Pedigree Prader-Willi Syndrome Gestational Age Cushing Syndrome Acute Coronary Syndrome Polycystic Ovary Syndrome Phenotype Williams Syndrome Chromosomes, Human, 1-3 DiGeorge Syndrome Klinefelter Syndrome Horner Syndrome Long QT Syndrome Craniofacial Abnormalities Guillain-Barre Syndrome Hemolytic-Uremic Syndrome Sex Chromosome Aberrations Compartment Syndromes Tourette Syndrome Cytogenetic Analysis Antiphospholipid Syndrome Heart Defects, Congenital Chromosome Deletion Abortion, Eugenic Cytogenetics Fetus Porcine Reproductive and Respiratory Syndrome Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 11 Carpal Tunnel Syndrome Werner Syndrome Reye Syndrome Forehead Mutation Bartter Syndrome Microcephaly Facies Porcine respiratory and reproductive syndrome virus Retrospective Studies Chromosomes, Human, Pair 15 HELLP Syndrome

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