Informaţii despre

Nume Autism
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Childhood autism
Clasificare anatomică Malacards Boli psihice
Boli din aceeaşi familie Autism 10; Autism 11; Autism 12; Autism 13; Autism 15; Autism 16; Autism 17; Autism 18; Autism 19; Autism 3; Autism 5; Autism 6; Autism 7; Autism 8; Autism 9; Autism Spectrum Disorder

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Boli A-Z 16p11.2 Duplication 16q24.3 Microdeletion Syndrome 2-Methylbutyryl-Coa Dehydrogenase Deficiency 7q11.23 Duplication Syndrome Aarskog-Scott Syndrome Achalasia Acrocallosal Syndrome Acromelic Frontonasal Dysostosis Acute Pancreatitis Adenylosuccinase Deficiency Adnp-Related Intellectual Disability and Autism Spectrum Disorder Adult Mesoblastic Nephroma Aging Agnosia Agoraphobia Alacrima, Achalasia, and Mental Retardation Syndrome Albinism Alcohol Abuse Alexithymia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amenorrhea Anauxetic Dysplasia 1 Angelman Syndrome Angelman Syndrome Due to Imprinting Defect in 15q11-Q13 Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antisocial Personality Disorder Anxiety Aphasia Apraxia Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Asperger Syndrome Asperger Syndrome 1 Asthma Astrocytoma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Septal Defect 1 Attention Deficit-Hyperactivity Disorder Atypical Autism Atypical Depressive Disorder Autism 11 Autism 12 Autism 13 Autism 3 Autism 5 Autism 6 Autism 7 Autism 8 Autism Spectrum Disorder Autoimmune Disease Autoimmune Lymphoproliferative Syndrome Autonomic Dysfunction Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Autosomal Dominant Non-Syndromic Intellectual Disability Axonal Neuropathy Bannayan-Riley-Ruvalcaba Syndrome Bardet-Biedl Syndrome Basal Ganglia Calcification Biotinidase Deficiency Bipolar Disorder Bipolar I Disorder Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Dysmorphic Disorder Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Borderline Personality Disorder Borna Disease Brain Injury Brainstem Auditory Evoked Responses Brunner Syndrome Bruxism Bulimia Nervosa 1 Camurati-Engelmann Disease Cdkl5-Related Disorder Central Nervous System Disease Cerebellar Atrophy, Developmental Delay, and Seizures Cerebellar Hypoplasia Cerebral Creatine Deficiency Syndrome 1 Cerebral Folate Deficiency Cerebral Palsy Cerebral Visual Impairment Cerebritis Cerebrotendinous Xanthomatosis Ceroid Lipofuscinosis, Neuronal, 8, Northern Epilepsy Variant Charge Syndrome Chiari Malformation Childhood Apraxia of Speech Childhood Disintegrative Disease Childhood-Onset Schizophrenia Chlamydia Chorioamnionitis Chromosomal Disease Chromosomal Triplication Chromosome 10p Deletion Chromosome 15q11.2 Deletion Syndrome Chromosome 15q13.3 Deletion Syndrome Chromosome 15q24 Deletion Syndrome Chromosome 15q Duplication Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome 16p Duplication Chromosome 22q11.2 Duplication Syndrome Chromosome 2p16.1-P15 Deletion Syndrome Chromosome Xp Deletion Chronic Fatigue Syndrome Clark-Baraitser Syndrome Classic Phenylketonuria Cognitive Function 1, Social Cohen Syndrome Colitis Collecting Duct Carcinoma Common Variable Immunodeficiency Conduct Disorder Congenital Contractures Congenital Cytomegalovirus Congenital Rubella Constipation Corneal Dystrophy Cornelia De Lange Syndrome Costello Syndrome Cranioectodermal Dysplasia 1 Craniosynostosis 1 Creatine Deficiency Syndromes Cri-Du-Chat Syndrome Cytochrome P450 2d6 Variant Cytomegalic Congenital Adrenal Hypoplasia Cytomegalovirus Infection Danon Disease Delusional Disorder Dermatitis Developmental Coordination Disorder Developmental Dyspraxia Disease of Mental Health Distal Trisomy 10q Down Syndrome Duane Retraction Syndrome 1 Dysautonomia Dysgraphia Dyskeratosis Congenita, X-Linked Dyslexia Dysphasia, Familial Developmental Early-Onset Schizophrenia Eating Disorder Echolalia Eclampsia Ehlers-Danlos Syndrome Encephalitis Encephalopathy Endogenous Depression Endotheliitis Eosinophilic Colitis Epilepsy Epileptic Encephalopathy, Early Infantile, 6 Expressive Language Disorder Fanconi Anemia, Complementation Group E Febrile Seizures Femoral-Facial Syndrome Fetal Alcohol Spectrum Disorder Fetal Alcohol Syndrome Fetishism Focal Epilepsy Foxp2-Related Speech and Language Disorders Fragile X Syndrome Galactose Epimerase Deficiency Gender Identity Disorder Generalized Anxiety Disorder Generalized Epilepsy with Febrile Seizures Plus Gianotti Crosti Syndrome Gilbert Syndrome Gilles De La Tourette Syndrome Gingivitis Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Hemifacial Atrophy, Progressive Hemihyperplasia, Isolated Hemochromatosis, Type 1 Hepatic Adenomas, Familial Hereditary Multiple Exostoses Hereditary Xanthinuria Heroin Dependence Herpes Simplex Herpes Simplex Encephalitis Histidinemia Hyperacusis Hyper Ige Syndrome Hyperinsulinemic Hypoglycemia, Familial, 6 Hyperlexia Hyperprolactinemia Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypervitaminosis a Hypoadrenocorticism, Familial Hypoascorbemia Hypocalcemia, Autosomal Dominant 1 Hypoganglionosis Hypoparathyroidism Hypophosphatemia Hypothalamic Hamartomas Hypotonia Hypotrichosis 1 Ichthyosis Ichthyosis, Congenital, Autosomal Recessive 11 Ileocolitis Immunoglobulin E Concentration, Serum Infertility Iqsec2 Isodicentric Chromosome 15 Syndrome Jacobsen Syndrome Juvenile Pilocytic Astrocytoma Kbg Syndrome Kidney Angiomyolipoma Kindler Syndrome Kleefstra Syndrome Kleine-Levin Hibernation Syndrome Kleptomania Kniest Dysplasia Landau-Kleffner Syndrome Langer Mesomelic Dysplasia Learning Disability Leopard Syndrome Leri-Weill Dyschondrosteosis Li-Fraumeni Syndrome Li-Fraumeni Syndrome 2 Linear Skin Defects with Multiple Congenital Anomalies 1 Lissencephaly Lissencephaly with Cerebellar Hypoplasia Lowe Oculocerebrorenal Syndrome Lubs X-Linked Mental Retardation Syndrome Lyme Disease Lymphoproliferative Syndrome Macrocephaly/autism Syndrome Macrocephaly, Benign Familial Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Major Affective Disorder 8 Major Affective Disorder 9 Malignant Spiradenoma Marchiafava Bignami Disease Marshall-Smith Syndrome Mbd5 Haploinsufficiency Measles Meckel Syndrome, Type 1 Megalencephaly Meningoencephalitis Mental Depression Mercury Poisoning Microcephaly Microcephaly 1, Primary, Autosomal Recessive Microphthalmia Migraine Without Aura Mitochondrial Disorders Mitochondrial Myopathy Mixed Receptive-Expressive Language Disorder Momo Syndrome Mood Disorder Mowat-Wilson Syndrome Mucopolysaccharidosis-Plus Syndrome Mucositis Mumps Mungan Syndrome Muscular Dystrophy Muscular Dystrophy, Duchenne Type Musical Perfect Pitch Mutism Myhre Syndrome Myopathy Myotonic Dystrophy Neonatal Hypoxic and Ischemic Brain Injury Neonatal Jaundice Nephrocalcinosis Nervous System Disease Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuroleptic Malignant Syndrome Neuronitis Neuropathy Nicolaides-Baraitser Syndrome Non-Syndromic Intellectual Disability Obesity, Hyperphagia, and Developmental Delay Obsessive-Compulsive Disorder Ocular Dominance Oculocerebral Syndrome with Hypopigmentation Oculocutaneous Albinism Opioid Addiction Oppositional Defiant Disorder Optic Nerve Hypoplasia, Bilateral Osteomyelitis Pancreatitis Panic Disorder Paragangliomas 1 Paranoid Schizophrenia Parkinson Disease 2, Autosomal Recessive Juvenile Parkinsonism with Spasticity, X-Linked Pathological Gambling Periodic Limb Movement Disorder Personality Disorder Pervasive Developmental Disorder Phelan-Mcdermid Syndrome Phenylketonuria Phobia, Specific Phobic Disorder Pilocytic Astrocytoma Pitt-Hopkins-Like Syndrome Pitt-Hopkins Syndrome Placental Insufficiency Pneumonia Polysubstance Abuse Porphyria Posterior Urethral Valves Postpartum Depression Post-Traumatic Stress Disorder Potocki-Lupski Syndrome Prader-Willi Syndrome Prader-Willi Syndrome Due to Imprinting Mutation Prader-Willi Syndrome Due to Maternal Uniparental Disomy of Chromosome 15 Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2 Pre-Eclampsia Priapism Propionic Acidemia Prosopagnosia Protocadherin-Alpha Gene Cluster Psychosexual Disorder Psychotic Disorder Retinitis Pigmentosa 42 Rett Syndrome Ring Chromosome 13 Ring Chromosome 17 Ring Chromosome 18 Ring Chromosome 22 Rubella Ruvalcaba Syndrome Schindler Disease Schizoaffective Disorder Schizophrenia Schizophrenia 1 Schizotypal Personality Disorder Seizure Disorder Sensorineural Hearing Loss Separation Anxiety Disorder Serotonin Syndrome Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Sleep Disorder Smith-Lemli-Opitz Syndrome Smith-Magenis Syndrome Social Phobia Sotos Syndrome 1 Spasticity Spastic Paraplegia 20, Autosomal Recessive Specific Developmental Disorder Specific Language Impairment Spondylocarpotarsal Synostosis Syndrome Spondyloocular Syndrome Status Epilepticus Strabismus Substance Abuse Substance Dependence Succinic Semialdehyde Dehydrogenase Deficiency Sudden Infant Death Syndrome Superior Mesenteric Artery Syndrome Syndromic Intellectual Disability Synesthesia Tardive Dyskinesia Testicular Regression Syndrome Tetrasomy 9p Thyroiditis Tic Disorder Timothy Syndrome Toxoplasmoză Trichotillomania Triple X Syndrome Tritanopia Tuberous Sclerosis Turner Syndrome Urethritis Vaccinia Valproate Embryopathy Velocardiofacial Syndrome Visual Agnosia Vohwinkel Syndrome, Variant Form West Syndrome Williams-Beuren Syndrome Witteveen-Kolk Syndrome Writing Disorder Xanthinuria Xanthinuria, Type Ii Xanthomatosis X-Linked Non-Specific Intellectual Disability Xp11.22 Deletion Yemenite Deaf-Blind Hypopigmentation Syndrome