Adults with 22q11 deletion syndrome. Medical search. Frequent questions

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Anatomy7

Chromosomes, Human, Pair 22 Parietal Bone Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 6 Branchial Region Brain Chromosomes, Human, Pair 18

Organisms2

Staphylococcus lugdunensis Mice, Inbred C57BL

Diseases40

22q11 Deletion Syndrome DiGeorge Syndrome Syndrome Chromosome Deletion Velopharyngeal Insufficiency Abnormalities, Multiple Craniofacial Abnormalities Chromosome Disorders Intellectual Disability Jacobsen Distal 11q Deletion Syndrome Hypoparathyroidism Cri-du-Chat Syndrome Facies Chromosome Breakage Hypocalcemia WAGR Syndrome Muscle Hypotonia Heart Defects, Congenital Eye Abnormalities Exostoses, Multiple Hereditary Learning Disorders Down Syndrome Metabolic Syndrome X Monosomy Language Development Disorders Chromosome Aberrations Cleft Palate Nephrotic Syndrome Growth Disorders Sjogren's Syndrome Translocation, Genetic Seizures Turner Syndrome Myelodysplastic Syndromes Genetic Predisposition to Disease Williams Syndrome Prader-Willi Syndrome Cushing Syndrome Acute Coronary Syndrome Polycystic Ovary Syndrome

Chemicals and Drugs3

Catechol O-Methyltransferase T-Box Domain Proteins Complement C1q

Analytical, Diagnostic and Therapeutic Techniques and Equipment12

In Situ Hybridization, Fluorescence Facies Karyotyping Comparative Genomic Hybridization Pedigree Chromosome Banding Chromosome Mapping Magnetic Resonance Imaging Case-Control Studies Genetic Association Studies Analysis of Variance DNA Mutational Analysis

Psychiatry and Psychology13

Intellectual Disability Developmental Disabilities Schizophrenia Stanford-Binet Test Learning Disorders Intelligence Tests Siblings Cognition Disorders Intelligence Neuropsychological Tests Psychotic Disorders Psychiatric Status Rating Scales Mental Disorders

Phenomena and Processes21

Chromosomes, Human, Pair 22 Chromosome Deletion Gene Deletion Sequence Deletion Phenotype Hemizygote Chromosome Breakage Mutation Monosomy Chromosome Aberrations Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 6 Genotype Base Sequence Gene Dosage Gene Rearrangement Translocation, Genetic Chromosomes, Human, Pair 18 Amino Acid Sequence Genetic Predisposition to Disease Polymorphism, Single Nucleotide

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups2

Infant, Newborn Siblings

Health Care2

Case-Control Studies Analysis of Variance

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

22q11 Deletion Syndrome DiGeorge Syndrome Chromosomes, Human, Pair 22 Syndrome Chromosome Deletion Velopharyngeal Insufficiency Gene Deletion Abnormalities, Multiple Craniofacial Abnormalities Chromosome Disorders Sequence Deletion Intellectual Disability Jacobsen Distal 11q Deletion Syndrome Hypoparathyroidism Developmental Disabilities Parietal Bone Cri-du-Chat Syndrome Phenotype Hemizygote In Situ Hybridization, Fluorescence Facies Chromosome Breakage Hypocalcemia Catechol O-Methyltransferase WAGR Syndrome Karyotyping Muscle Hypotonia Schizophrenia Heart Defects, Congenital Eye Abnormalities T-Box Domain Proteins Stanford-Binet Test Exostoses, Multiple Hereditary Learning Disorders Down Syndrome Metabolic Syndrome X Mutation Molecular Sequence Data Monosomy Language Development Disorders Comparative Genomic Hybridization Chromosome Aberrations Pedigree Chromosome Banding Chromosome Mapping Chromosomes, Human, Pair 1 Staphylococcus lugdunensis Chromosomes, Human, Pair 6 Branchial Region Cleft Palate Intelligence Tests Genotype Base Sequence Brain Infant, Newborn Gene Dosage Nephrotic Syndrome Magnetic Resonance Imaging Siblings Growth Disorders Sjogren's Syndrome Gene Rearrangement Cognition Disorders Translocation, Genetic Case-Control Studies Intelligence Chromosomes, Human, Pair 18 Neuropsychological Tests Seizures Genetic Association Studies Psychotic Disorders Turner Syndrome Psychiatric Status Rating Scales Myelodysplastic Syndromes Amino Acid Sequence Genetic Predisposition to Disease Williams Syndrome Complement C1q Polymorphism, Single Nucleotide Prader-Willi Syndrome Cushing Syndrome Mice, Inbred C57BL Mental Disorders Analysis of Variance DNA Mutational Analysis Acute Coronary Syndrome Polycystic Ovary Syndrome

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