Informaţii despre

Nume Schizophrenia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Schizophrenia, unspecified
Clasificare anatomică Malacards Boli neuronale; Boli psihice
Boli din aceeaşi familie Early-Onset Schizophrenia; Schizophrenia 1; Schizophrenia 10; Schizophrenia 11; Schizophrenia 12; Schizophrenia 13; Schizophrenia 14; Schizophrenia 15; Schizophrenia 16; Schizophrenia 18; Schizophrenia 19; Schizophrenia 2; Schizophrenia 3; Schizophrenia 4; Schizophrenia 5; Schizophrenia 6; Schizophrenia 7; Schizophrenia 8; Schizophrenia 9

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Boli A-Z 17q12 Duplication Aceruloplasminemia Acid-Labile Subunit Deficiency Acrocallosal Syndrome Acute Leukemia of Ambiguous Lineage Acute Necrotizing Encephalopathy Aging Agnosia Agoraphobia Aids Dementia Complex Akinetic Mutism Albinism Alcohol Abuse Alcohol Dependence Alcohol Use Disorder Alexithymia Alopecia 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 Alzheimer Disease 5 Amenorrhea Amnestic Disorder Amphetamine Abuse Amusia Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Anosognosia Antisocial Personality Disorder Anxiety Aortic Valve Disease 2 Aplasia of Lacrimal and Salivary Glands Appendicitis Arachnoid Cysts Arachnoiditis Argyria Arterial Tortuosity Syndrome Arteries, Anomalies of Arteriosclerosis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy, Progressive Pseudorheumatoid, of Childhood Asperger Syndrome Asplenia, Isolated Congenital Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Atrial Septal Defect 1 Attention Deficit-Hyperactivity Disorder Atypical Depressive Disorder Aural Atresia, Congenital Autism Autism Spectrum Disorder Autoimmune Polyendocrine Syndrome Type 1 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia Autoimmune Polyglandular Syndrome Type 3 Autonomic Dysfunction Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Avoidant Personality Disorder Axenfeld-Rieger Syndrome Basal Ganglia Calcification Beriberi Beta-Thalassemia Bipolar Disorder Bipolar I Disorder Bleeding Disorder, Platelet-Type, 11 Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Dysmorphic Disorder Body Mass Index Quantitative Trait Locus 1 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 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Borderline Personality Disorder Borna Disease Brain Injury Brain Ischemia Brainstem Auditory Evoked Responses Breast Cancer Brunner Syndrome Bulimia Nervosa 1 Bulimia Nervosa 2 Bullous Skin Disease Cannabis Abuse Cannabis Dependence Capgras Syndrome Cataract 5, Multiple Types Cat Eye Syndrome Celiac Disease 1 Central Nervous System Disease Centralopathic Epilepsy Central Pontine Myelinolysis Cerebellar Atrophy, Developmental Delay, and Seizures Cerebellar Degeneration Cerebral Arteriosclerosis Cerebral Atrophy Cerebral Folate Deficiency Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Ceroid Lipofuscinosis, Neuronal, 5 Chilaiditi Syndrome Childhood-Onset Schizophrenia Cholecystitis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choroiditis Chromosomal Triplication Chromosome 15q13.3 Deletion Syndrome Chromosome 22q11.2 Duplication Syndrome Chromosome 2p16.3 Deletion Syndrome Chromosome 3q29 Deletion Syndrome Chronic Fatigue Syndrome Citrullinemia, Classic Cocaine Abuse Cocaine Dependence Coffin-Lowry Syndrome Cognitive Function 1, Social Colitis Colorectal Cancer Communicating Hydrocephalus Complement Component 4b Deficiency Conduct Disorder Constipation Cortical Blindness Cranioectodermal Dysplasia 1 Craniosynostosis with Fibular Aplasia Cutis Verticis Gyrata Cytochrome P450 2d6 Variant Cytomegalovirus Infection Dandy-Walker Complex Darier-White Disease Delusional Disorder Dementia Dental Caries Dependent Personality Disorder Developmental Coordination Disorder Diabetes Mellitus Dicarboxylic Aminoaciduria Digeorge Syndrome Dihydropyrimidinase Deficiency Disease of Mental Health Dissociative Disorder Down Syndrome Drug Dependence Drug-Induced Mental Disorder Drug Psychosis Dumping Syndrome Duodenal Obstruction Duodenitis Dyskeratosis Congenita Dyskinesia of Esophagus Dyslexia Dyspepsia Dysphasia, Familial Developmental Dystonia Early-Onset Schizophrenia Eating Disorder Elective Mutism Emphysematous Cholecystitis Encephalitis Encephalomalacia Encephalopathy Endogenous Depression Endotheliitis Epilepsy Episodic Ataxia Episodic Ataxia, Type 2 Epithelial Recurrent Erosion Dystrophy Exostosis Exotropia Factitious Disorder Familial Adenomatous Polyposis Familial Idiopathic Basal Ganglia Calcification Fanconi Anemia, Complementation Group E Febrile Seizures Fetal Alcohol Syndrome Focal Epilepsy Fontaine Progeroid Syndrome Fragile X Syndrome Frontotemporal Dementia Fryns Syndrome Galactorrhea Galactorrhoea-Hyperprolactinaemia Galactosemia Gastroparesis Gender Identity Disorder Generalized Anxiety Disorder Gilles De La Tourette Syndrome Gitelman Syndrome Glioblastoma Glomerulonephritis Granulocytopenia Graves' Disease Hair Whorl Hantavirus Pulmonary Syndrome Headache Helix Syndrome Hemophilia Hemophilia a Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatitis C Hepatitis C Virus Hepatitis E Hereditary Multiple Exostoses Hereditary Wilms' Tumor Hermansky-Pudlak Syndrome Heroin Dependence Herpes Simplex Homocysteinemia Homocystinuria Hydrocephalus Hyperandrogenism Hyperphenylalaninemia Hyperprolactinemia Hyperprolinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoascorbemia Hypocalcemia, Autosomal Dominant 1 Hypochondriasis Hypoglycemic Coma Hypoparathyroidism Hypoxia Ichthyosis Prematurity Syndrome Influenza Intermittent Explosive Disorder Intraventricular Meningioma Ischemia Isolated Optic Neuritis Kallmann Syndrome Kleine-Levin Hibernation Syndrome Kleptomania Klippel-Feil Syndrome Koro Lateral Sclerosis Learning Disability Leigh Syndrome Leukemia Leukodystrophy Leukomalacia Lingual-Facial-Buccal Dyskinesia Lissencephaly Lissencephaly 1 Liver Disease Lujan-Fryns Syndrome Lung Cancer Lupus Erythematosus Lymphoma Macs Syndrome Major Affective Disorder 3 Major Affective Disorder 8 Major Affective Disorder 9 Major Depressive Disorder Malignant Hyperthermia Malignant Spiradenoma Marfan Syndrome Mcleod Syndrome Meckel Syndrome, Type 1 Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 Megaloblastic Anemia Melancholia Meningioma, Familial Meningitis Mental Depression Metachromatic Leukodystrophy Microcephaly Microscopic Polyangiitis Middle Ear Disease Migraine with Aura Migraine Without Aura Milia, Multiple Eruptive Moebius Syndrome Mood Disorder Motor Neuron Disease Mthfr Gene Variant Mucopolysaccharidosis, Type Vii Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Personality Disorder Multiple Sclerosis Multiple System Atrophy 1 Mungan Syndrome Muscular Dystrophy Mutism Myasthenia Gravis Myeloid Leukemia Myocarditis Myoclonus Myopathy Myxedema N Acetyltransferase Deficiency Narcolepsy Neonatal Hypoxic and Ischemic Brain Injury Netherton Syndrome Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurodegeneration with Brain Iron Accumulation 2a Neuroleptic Malignant Syndrome Neuronal Migration Disorders Neuronitis Neurosarcoidosis Neurosyphilis Neurotic Disorder Neutropenia Neutrophil Actin Dysfunction Niemann-Pick Disease Obsessive-Compulsive Disorder Ocular Dominance Ocular Motor Apraxia Ocular Toxoplasmosis Oculocutaneous Albinism Olfactory Groove Meningioma Oligospermia Opiate Dependence Opioid Abuse Opioid Addiction Oppositional Defiant Disorder Osteomyelitis Pachyonychia Congenita 2 Pancreatitis Pancytopenia Panencephalitis, Subacute Sclerosing Panic Disorder Papilloma Paragangliomas 1 Paralytic Ileus Parametritis Paranoid Personality Disorder Paranoid Schizophrenia Parathyroid Carcinoma Pathological Gambling Pellagra Pemphigus Pericardial Effusion Periodic Limb Movement Disorder Peripartum Cardiomyopathy Periventricular Leukomalacia Personality Disorder Pervasive Developmental Disorder Phelan-Mcdermid Syndrome Phencyclidine Abuse Phosphoglycerate Dehydrogenase Deficiency Pick Disease of Brain Pitt-Hopkins-Like Syndrome Pitt-Hopkins Syndrome Pituitary Stalk Interruption Syndrome Placental Insufficiency Platelet-Activating Factor Acetylhydrolase Deficiency Pneumonia Polymorphic Reticulosis Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes Polysubstance Abuse Porphyria Postpartum Depression Post-Traumatic Stress Disorder Premature Ejaculation Priapism Prieto X-Linked Mental Retardation Syndrome Progressive Multifocal Leukoencephalopathy Prosopagnosia Prostatitis Psychosexual Disorder Psychotic Disorder Pure Autonomic Failure Restless Legs Syndrome Retinitis Retinitis Pigmentosa Retinoschisis 1, X-Linked, Juvenile Rheumatoid Arthritis Rubella Schizencephaly Schizoaffective Disorder Schizophrenia 1 Schizophrenia 10 Schizophrenia 11 Schizophrenia 12 Schizophrenia 13 Schizophrenia 14 Schizophrenia 2 Schizophrenia 3 Schizophrenia 4 Schizophrenia 5 Schizophrenia 6 Schizophrenia 7 Schizophrenia 8 Schizophreniform Disorder Schizotypal Personality Disorder Seizure Disorder Separation Anxiety Disorder Serotonin Syndrome Severe Hemophilia a Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Skin Disease Sleep Apnea Smith-Kingsmore Syndrome Smoking As a Quantitative Trait Locus 3 Social Phobia Spastic Paraplegia 20, Autosomal Recessive Specific Language Impairment Speech Disorder Spinocerebellar Ataxia 2 Spinocerebellar Ataxia 6 Spondyloocular Syndrome Squamous Cell Carcinoma Status Epilepticus Strabismus Stuttering Substance Abuse Substance Dependence Substance-Induced Psychosis Swallowing Disorders Syndrome of Inappropriate Antidiuretic Hormone Synucleinopathy Syringocystadenoma Papilliferum Systemic Lupus Erythematosus Takenouchi-Kosaki Syndrome Taqi Polymorphism Tardive Dyskinesia Tarp Syndrome Tay-Sachs Disease T Cell Deficiency Temporal Lobe Epilepsy Testicular Regression Syndrome Tetralogy of Fallot Thalassemia Thiourea Tasting Thrombocytopenia 1 Thyroid Crisis Thyroiditis Tibia, Hypoplasia or Aplasia of, with Polydactyly Tic Disorder Tobacco Addiction Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Toxic Encephalopathy Toxicity or Absent Response to Clozapine Toxoplasmoză Transsexualism Transsexuality Traumatic Brain Injury Treacher Collins Syndrome 1 Trichotillomania Tritanopia Turner Syndrome Ulcerative Colitis Usher Syndrome Vascular Dementia Vascular Disease Velocardiofacial Syndrome Williams-Beuren Syndrome Wilson Disease Wolff-Parkinson-White Syndrome Wolfram Syndrome X-Ray Sensitivity Yemenite Deaf-Blind Hypopigmentation Syndrome