Mental retardation. Medical search. Frequent questions

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Anatomy41

Chromosomes, Human, X X Chromosome Face Brain Ring Chromosomes Facial Bones Chromosomes, Human, Pair 15 Neurons Chromosomes, Human, Pair 21 Dendritic Spines Dendrites Chromosomes, Human, 6-12 and X Toes Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 16 Telomere Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 2 Hippocampus Synapses Chromosomes, Human, Pair 4 Chromosomes, Human, 1-3 Polyribosomes Parietal Bone Chromosomes, Human, 4-5 Chromosomes, Artificial, Yeast Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 18 Chromosomes, Human, 13-15 Chromosomes, Human, Pair 9 Mushroom Bodies Skull Cerebellum Chromosomes, Human, Pair 1 Intranuclear Inclusion Bodies Chromosomes, Human, Pair 3 Cell Line Chromosomes, Human, Pair 13 Cells, Cultured Chromosomes, Human, Pair 7 Chromosomes, Artificial, P1 Bacteriophage

Organisms3

Mice, Knockout Mice, Inbred C57BL Drosophila

Diseases100

Intellectual Disability Mental Retardation, X-Linked Fragile X Syndrome Abnormalities, Multiple Syndrome Microcephaly Sex Chromosome Aberrations Fetal Growth Retardation Facies Growth Disorders Ataxia Chromosome Deletion Rett Syndrome Spasms, Infantile Muscle Hypotonia Chromosome Disorders Chromosome Aberrations Craniofacial Abnormalities Down Syndrome Epilepsy Hypertelorism alpha-Thalassemia Psychomotor Disorders Trisomy Ring Chromosomes Hand Deformities, Congenital Coloboma Nervous System Malformations Oculocerebrorenal Syndrome Translocation, Genetic Tuberous Sclerosis Monosomy Seizures Rubinstein-Taybi Syndrome Angelman Syndrome Chromosome Breakage Genetic Diseases, X-Linked Phenylketonurias Cerebellar Ataxia Coffin-Lowry Syndrome Language Development Disorders Chromosome Fragility Failure to Thrive WAGR Syndrome Learning Disorders Sex Chromosome Disorders Classical Lissencephalies and Subcortical Band Heterotopias Sjogren-Larsson Syndrome Wolf-Hirschhorn Syndrome Agenesis of Corpus Callosum Bone Diseases, Developmental Lissencephaly Ichthyosis Disease Models, Animal Foot Deformities, Congenital Dwarfism Cri-du-Chat Syndrome Tremor Syndactyly Chromosome Inversion Eye Abnormalities Smith-Lemli-Opitz Syndrome De Lange Syndrome Congenital Hypothyroidism Bardet-Biedl Syndrome Tooth Abnormalities Urogenital Abnormalities Genetic Diseases, Inborn Cerebral Palsy Williams Syndrome Fetal Alcohol Spectrum Disorders Phenylketonuria, Maternal Congenital Abnormalities Hypogonadism Laurence-Moon Syndrome Prader-Willi Syndrome Craniofacial Dysostosis Methemoglobinemia Nervous System Diseases Blepharoptosis Musculoskeletal Abnormalities Hydrocephalus Metabolism, Inborn Errors Heredodegenerative Disorders, Nervous System Chorea Gravidarum Deafness Homocystinuria alpha-Mannosidosis Orofaciodigital Syndromes Pain Insensitivity, Congenital Sexual Infantilism Heart Defects, Congenital DiGeorge Syndrome Muscular Dystrophies Amino Acid Metabolism, Inborn Errors Microphthalmos Blepharophimosis Cleft Palate Abnormalities, Drug-Induced Hearing Disorders

Chemicals and Drugs28

Fragile X Mental Retardation Protein Methyl-CpG-Binding Protein 2 RNA-Binding Proteins Nerve Tissue Proteins Hemoglobin H Interleukin-1 Receptor Accessory Protein Codon, Nonsense Nuclear Proteins Receptors, Metabotropic Glutamate Genetic Markers Adaptor Protein Complex sigma Subunits RNA, Messenger Receptor, Metabotropic Glutamate 5 Methoxyhydroxyphenylglycol Drosophila Proteins DNA-Binding Proteins Glutethimide Transcription Factors DNA Repressor Proteins DNA Helicases DNA Primers GTPase-Activating Proteins Azure Stains RNA Adenylosuccinate Lyase Histone Demethylases Guanylate Kinase

Analytical, Diagnostic and Therapeutic Techniques and Equipment20

Pedigree Facies Karyotyping In Situ Hybridization, Fluorescence Chromosome Banding Chromosome Mapping DNA Mutational Analysis Heterozygote Detection Genetic Testing Disease Models, Animal Comparative Genomic Hybridization Dermatoglyphics Dental Care for Disabled Physical Chromosome Mapping Polymerase Chain Reaction Rehabilitation, Vocational Magnetic Resonance Imaging Cytogenetic Analysis Prenatal Diagnosis Sequence Analysis, DNA

Psychiatry and Psychology17

Intellectual Disability Developmental Disabilities Education of Intellectually Disabled Autistic Disorder Psychomotor Disorders Intelligence Tests Intelligence Learning Disorders Projective Techniques Generalization (Psychology)Nail Biting Schizophrenia, Childhood Behavior Therapy Self-Injurious Behavior Stereotypic Movement Disorder Reinforcement (Psychology)Cognition Disorders

Phenomena and Processes74

Sex Chromosome Aberrations Chromosomes, Human, X X Chromosome Consanguinity Chromosome Deletion Phenotype Mutation Genetic Linkage Genes, Recessive Chromosome Aberrations Base Sequence Trisomy Ring Chromosomes Heterozygote Trinucleotide Repeat Expansion Pregnancy Translocation, Genetic Dosage Compensation, Genetic Monosomy Chromosome Breakage Chromosomes, Human, Pair 15 Gene Duplication Gene Deletion Codon, Nonsense Chromosomes, Human, Pair 21 Mutation, Missense Amino Acid Sequence Chromosome Fragility Genetic Markers Chromosomes, Human, 6-12 and X Gene Dosage Sequence Deletion Homozygote Chromosomes, Human, Pair 8 Mosaicism Chromosome Inversion Trinucleotide Repeats Chromosomes, Human, Pair 16 Telomere Chromosomes, Human, Pair 22 Exons Chromosomes, Human, Pair 2 X Chromosome Inactivation Genes, X-Linked Chromosome Fragile Sites Chromosomes, Human, Pair 4 Chromosomes, Human, 1-3 Frameshift Mutation Lod Score Birefringence Protein Biosynthesis Microsatellite Repeats Gene Expression Regulation Chromosomes, Human, 4-5 Chromosomes, Artificial, Yeast Chromosomes, Human, Pair 17 Alleles Chromosomes, Human, Pair 18 Chromosomes, Human, 13-15 Chromosomes, Human, Pair 9 Protein Binding Haplotypes Genotype Chromosomes, Human, Pair 1 Gene Expression Regulation, Developmental Genes, Dominant Sequence Homology, Amino Acid Neuronal Plasticity Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 13 Inheritance Patterns Chromosomes, Human, Pair 7 Protein Structure, Tertiary Chromosomes, Artificial, P1 Bacteriophage

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Education of Intellectually Disabled Dermatoglyphics

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups2

Infant, Newborn Mentally Disabled Persons

Health Care6

Genetic Testing Group Homes Dental Care for Disabled Genetic Counseling Rehabilitation, Vocational Family Health

Geographicals3

Georgia Tunisia Oman

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

Intellectual Disability Mental Retardation, X-Linked Fragile X Mental Retardation Protein Fragile X Syndrome Abnormalities, Multiple Syndrome Microcephaly Pedigree Sex Chromosome Aberrations Fetal Growth Retardation Chromosomes, Human, X X Chromosome Facies Growth Disorders Consanguinity Ataxia Developmental Disabilities Chromosome Deletion Phenotype Mutation Education of Intellectually Disabled Methyl-CpG-Binding Protein 2 Karyotyping Genetic Linkage In Situ Hybridization, Fluorescence Rett Syndrome Genes, Recessive RNA-Binding Proteins Spasms, Infantile Muscle Hypotonia Chromosome Disorders Autistic Disorder Chromosome Banding Molecular Sequence Data Chromosome Aberrations Craniofacial Abnormalities Down Syndrome Chromosome Mapping Epilepsy Hypertelorism Face Base Sequence alpha-Thalassemia Infant, Newborn Nerve Tissue Proteins Psychomotor Disorders Trisomy Intelligence Tests Brain Ring Chromosomes DNA Mutational Analysis Hand Deformities, Congenital Heterozygote Coloboma Trinucleotide Repeat Expansion Hemoglobin H Nervous System Malformations Pregnancy Oculocerebrorenal Syndrome Translocation, Genetic Heterozygote Detection Tuberous Sclerosis Facial Bones Interleukin-1 Receptor Accessory Protein Dosage Compensation, Genetic Monosomy Seizures Rubinstein-Taybi Syndrome Angelman Syndrome Chromosome Breakage Intelligence Chromosomes, Human, Pair 15 Genetic Diseases, X-Linked Genetic Testing Neurons Mice, Knockout Gene Duplication Phenylketonurias Cerebellar Ataxia Gene Deletion Coffin-Lowry Syndrome Language Development Disorders Codon, Nonsense Chromosomes, Human, Pair 21 Mutation, Missense Amino Acid Sequence Nuclear Proteins Chromosome Fragility Receptors, Metabotropic Glutamate Failure to Thrive Genetic Markers Dendritic Spines WAGR Syndrome Learning Disorders Sex Chromosome Disorders Classical Lissencephalies and Subcortical Band Heterotopias Dendrites Sjogren-Larsson Syndrome Wolf-Hirschhorn Syndrome Adaptor Protein Complex sigma Subunits

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