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Nume Encephalopathy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Encephalopathy, unspecified
Clasificare anatomică Malacards Boli ale ochiului; Boli neuronale
Boli din aceeaşi familie Encephalopathy Due to Defective Mitochondrial and Peroxisomal Fission 1; Encephalopathy Due to Defective Mitochondrial and Peroxisomal Fission 2

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Boli A-Z 2-Hydroxyglutaric Aciduria 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 3-Methylcrotonyl-Coa Carboxylase Deficiency 3-Methylglutaconic Aciduria 3-Methylglutaconic Aciduria, Type Iv 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome 5-Oxoprolinase Deficiency 5q31.3 Microdeletion Syndrome Abdominal Tuberculosis Ablepharon-Macrostomia Syndrome Acetyl-Carnitine Deficiency Achalasia Acquired Immunodeficiency Syndrome Acute Chest Syndrome Acute Disseminated Encephalomyelitis Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion Acute Liver Failure Acute Motor and Sensory Axonal Neuropathy Acute Myocardial Infarction Acute Necrotizing Encephalitis Acute Necrotizing Encephalopathy Acute Necrotizing Encephalopathy Type 1 Acute Pancreatitis Acute Porphyria Acute Poststreptococcal Glomerulonephritis Acute Transverse Myelitis Adenoma Adenylosuccinase Deficiency Adie Pupil Adrenal Adenoma Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency African Tick-Bite Fever Agammaglobulinemia Aging Agraphia Aicardi-Goutieres Syndrome Aicardi-Goutieres Syndrome 2 Aicardi-Goutieres Syndrome 3 Aicardi-Goutieres Syndrome 4 Aicardi-Goutieres Syndrome 5 Aicardi Syndrome Aids Dementia Complex Alcohol Abuse Alcoholic Hepatitis Alcoholic Liver Cirrhosis Alcohol-Related Neurodevelopmental Disorder Alcohol Use Disorder Alexander Disease Alexia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Methylacetoacetic Aciduria Alpha-Methylacyl-Coa Racemase Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alternating Hemiplegia of Childhood Alzheimer Disease 3 Amelogenesis Imperfecta Aminoaciduria Amyloidosis Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aneurysm Angelman Syndrome Angiomatosis Aniridia 1 Anorexia Nervosa 1 Anoxia Anterograde Amnesia Aortic Aneurysm Aortic Valve Disease 2 Aphasia Aplastic Anemia Apolipoprotein C-Ii Deficiency Arachnoid Cysts Arachnoiditis Argininosuccinic Aciduria Aromatic L-Amino Acid Decarboxylase Deficiency Arteriosclerosis Arteriovenous Fistula Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Asparagine Synthetase Deficiency Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Athetosis Autism Autoimmune Autonomic Ganglionopathy Autoimmune Disease Autoimmune Encephalitis Autoimmune Lymphoproliferative Syndrome Autonomic Dysfunction Autonomic Neuropathy Axonal Neuropathy Bacterial Meningitis Balint Syndrome Banti's Syndrome Basal Ganglia Disease B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Lymphomas Behr Syndrome Beriberi Biliary Atresia Binswanger's Disease Biotinidase Deficiency Bleeding Disorder, Platelet-Type, 11 Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blue Rubber Bleb Nevus 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 Boutonneuse Fever Brain Edema Brain Injury Brain Ischemia Brain Small Vessel Disease with or Without Ocular Anomalies Branchiootic Syndrome 1 Branch Retinal Artery Occlusion Brown-Sequard Syndrome Budd-Chiari Syndrome Bullous Pemphigoid Burns C1q Deficiency Capillary Leak Syndrome Cardiac Tamponade Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Carnitine Acetyltransferase Deficiency Carotid Artery Dissection Cataract Cat Eye Syndrome Cat-Scratch Disease Cdkl5-Related Disorder Central Nervous System Lymphoma Central Pontine Myelinolysis Cerebellar Atrophy, Developmental Delay, and Seizures Cerebellar Degeneration Cerebellar Hypoplasia Cerebral Arteriosclerosis Cerebral Atherosclerosis Cerebral Atrophy Cerebral Beriberi Cerebral Creatine Deficiency Syndrome 1 Cerebral Creatine Deficiency Syndrome 2 Cerebral Degeneration Cerebral Folate Deficiency Cerebral Hemorrhage Cerebral Hypoxia Cerebral Lymphoma Cerebral Palsy Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Cerebrocostomandibular Syndrome Cerebrospinal Fluid Leak Cervicitis Chd2 Myoclonic Encephalopathy Chikungunya Childhood Leukemia Cholesterol Embolism Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Chorioamnionitis Choroiditis Chronic Active Epstein-Barr Virus Infection Chronic Fatigue Syndrome Chronic Pain Chronic Progressive External Ophthalmoplegia Chronic Wasting Disease Chylomicron Retention Disease Cirrhosis, Familial Citrullinemia, Type Ii, Adult-Onset Citrullinemia, Type Ii, Neonatal-Onset Combined D-2- and L-2-Hydroxyglutaric Aciduria Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Conduct Disorder Congenital Disorder of Glycosylation, Type Ia Congenital Extrahepatic Portosystemic Shunt Congenital Nonhemolytic Jaundice Congenital Portosystemic Shunt Congenital Rubella Connective Tissue Disease Constipation Constrictive Pericarditis Corneal Dystrophy, Thiel-Behnke Type Cornelia De Lange Syndrome Corpus Callosum, Agenesis of, with Abnormal Genitalia Cortical Blindness Corticobasal Degeneration Cranioectodermal Dysplasia 1 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniosynostosis 1 Crescentic Glomerulonephritis Creutzfeldt-Jakob Disease Critical Illness Polyneuropathy Crouzon Syndrome with Acanthosis Nigricans Cryptococcal Meningitis Cyclic Vomiting Syndrome Cystinosis Cytomegalovirus Infection Dementia Dengue Hemorrhagic Fever Dengue Shock Syndrome Diabetes Insipidus Diabetes Mellitus Diabetic Encephalopathy Diarrhea Diarrhea 5, with Tufting Enteropathy, Congenital Diffuse Large B-Cell Lymphoma Digitalis Poisoning Dilated Cardiomyopathy Diphtheria Discoid Lupus Erythematosus Disseminated Intravascular Coagulation Donnai-Barrow Syndrome Duodenitis Dysautonomia Dysgraphia Dystonia Early Myoclonic Encephalopathy Eclampsia Ectodermal Dysplasia Encephalitis Encephalopathy, Acute, Infection-Induced 4 Encephalopathy, Ethylmalonic Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Encephalopathy, Progressive, with or Without Lipodystrophy Endotheliitis Eosinophilia-Myalgia Syndrome Eosinophilic Fasciitis Ependymoma Epidermolysis Bullosa Epilepsy Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation Epilepsy with Generalized Tonic-Clonic Seizures Epileptic Encephalopathy, Early Infantile, 15 Epileptic Encephalopathy, Early Infantile, 3 Epileptic Encephalopathy, Early Infantile, 4 Epileptic Encephalopathy, Early Infantile, 6 Epileptic Encephalopathy, Early Infantile, 7 Epileptic Encephalopathy, Early Infantile, 9 Epithelial Recurrent Erosion Dystrophy Erythema Infectiosum Erythema Multiforme Exanthem Exanthema Subitum Extrapontine Myelinolysis Extrapulmonary Tuberculosis Fabry Disease Factor X Deficiency Familial Acute Necrotizing Encephalopathy Familial Hemiplegic Migraine Familial Mediterranean Fever Fanconi Anemia, Complementation Group E Fasciitis Fatal Familial Insomnia Febrile Infection-Related Epilepsy Syndrome Febrile Seizures Ferro-Cerebro-Cutaneous Syndrome Fetal Akinesia Deformation Sequence Fetal Erythroblastosis Focal Epilepsy Focal Segmental Glomerulosclerosis Fumarase Deficiency Galactose Epimerase Deficiency Galactosemia Galloway-Mowat Syndrome Ganglioneuroblastoma Gastric Cancer Gastroparesis Glomerulonephritis Glutaric Acidemia I Glycine Encephalopathy Glycine Encephalopathy with Normal Serum Glycine Glyt1 Encephalopathy Gnao1 Encephalopathy Goodpasture Syndrome Graves' Disease Growth Hormone Deficiency Guillain-Barre Syndrome Hashimoto's Encephalitis Hashimoto Thyroiditis Headache Head Injury Helicobacter Pylori Infection Helix Syndrome Hellp Syndrome Hematopoietic Stem Cell Transplantation Hemimegalencephaly Hemiplegia Hemiplegic Migraine Hemochromatosis, Neonatal Hemoglobinuria Hemolytic Anemia Hemolytic-Uremic Syndrome Hemophagocytic Lymphohistiocytosis Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Hemorrhagic Shock and Encephalopathy Syndrome Hepatic Adenomas, Familial Hepatic Coma Hepatic Encephalopathy Hepatic Infarction Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis E Hepatoblastoma Hepatocellular Carcinoma Hereditary Ataxia Hereditary Spherocytosis Herpes Simplex Herpes Simplex Encephalitis Hhv-6 Encephalitis Histidinemia Histiocytosis Histoplasmosis Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Human Coronavirus Sensitivity Human Immunodeficiency Virus Type 1 Hydranencephaly Hydrocephalus Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Familial Hyperekplexia Hypereosinophilic Syndrome Hyperglycemia Hyperlipoproteinemia, Type I Hypermethioninemia Hyperphenylalaninemia Hypersomnia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hyperthyroidism Hypertonia Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoascorbemia Hypoglycemia Hypokalemia Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Hypopituitarism Hypotonia Hypoxia Idiopathic Hemiconvulsion-Hemiplegia Syndrome Immune Deficiency Disease Incontinentia Pigmenti Infancy Electroclinical Syndrome Infantile Epileptic Encephalopathy Infantile Glycine Encephalopathy Inflammatory Bowel Disease Influenza Inherited Metabolic Disorder Insulinoma Internuclear Ophthalmoplegia Intestinal Pseudo-Obstruction Intracranial Aneurysm Intracranial Embolism Intracranial Hypertension Intracranial Hypotension Intranuclear Rod Myopathy Intravascular Large B-Cell Lymphoma Ischemia Ischemic Optic Neuropathy Japanese Encephalitis Jeavons Syndrome Juvenile Rheumatoid Arthritis Kawasaki Disease Kearns-Sayre Syndrome Kernicterus Kleine-Levin Hibernation Syndrome Kuru L-2-Hydroxyglutaric Aciduria Lactic Acidosis Landau-Kleffner Syndrome Larsen Syndrome Laryngeal Adductor Paralysis Lassa Fever Lateral Sclerosis Leber Hereditary Optic Neuropathy Legius Syndrome Leigh Syndrome Lennox-Gastaut Syndrome Leukemia Leukomalacia Limbic Encephalitis Lipodystrophy Lipomatosis Liver Cirrhosis Liver Disease Localized Scleroderma Loeys-Dietz Syndrome Lung Cancer Lupus Erythematosus Lyme Disease Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoid Interstitial Pneumonia Lymphoma Lymphoproliferative Syndrome Lysinuric Protein Intolerance Lysosomal Storage Disease Malaria Malignant Hypertension Malignant Migrating Partial Seizures of Infancy Malignant Spiradenoma Maple Syrup Urine Disease Marchiafava Bignami Disease Meckel Syndrome, Type 1 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency Megaloblastic Anemia Melanoma Melkersson-Rosenthal Syndrome Membranoproliferative Glomerulonephritis Meningitis Meningoencephalitis Meningothelial Meningioma Mental Retardation, X-Linked, Syndromic, Hedera Type Metabolic Acidosis Mevalonic Aciduria Microcephaly Microcolon Microscopic Polyangiitis Middle Cerebral Artery Infarction Migraine with Aura Miller Fisher Syndrome Mitochondrial Complex I Deficiency Mitochondrial Disorders Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Dna Depletion Syndrome 9 Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mitochondrial Neurogastrointestinal Encephalopathy Disease Mixed Connective Tissue Disease Molybdenum Cofactor Deficiency Monoclonal Paraproteinemia Monocytic Leukemia Morbid Obesity Motor Neuron Disease Mucositis Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Chemical Sensitivity Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Multiple Sclerosis Multiple Symmetrical Lipomatosis Multiple System Atrophy 1 Mumps Muscular Atrophy Muscular Dystrophy Mutism Myelitis Myeloma, Multiple Myhre Syndrome Myocardial Infarction Myocarditis Myoclonic Astatic Epilepsy Myoclonic Encephalopathy of Infants Myoclonus Myoclonus Epilepsy Myoglobinuria Myoglobinuria, Acute Recurrent, Autosomal Recessive Myoma Myopathy Myositis Myxedema N-Acetylglutamate Synthase Deficiency Narcolepsy Neonatal Glycine Encephalopathy Neonatal Hypoxic and Ischemic Brain Injury Neonatal Jaundice Neonatal Period Electroclinical Syndrome Neonatal Stroke Neonatal Thyrotoxicosis Nephronophthisis Nephrotic Syndrome Neuroaxonal Dystrophy Neuroblastoma Neurodegeneration with Brain Iron Accumulation 5 Neuroendocrine Tumor Neuroleptic Malignant Syndrome Neuromuscular Disease Neuromyelitis Optica Neuromyelitis Optica Spectrum Disorder Neuronitis Neuropathy Neuroretinitis Neurosarcoidosis Neurosyphilis Nodular Regenerative Hyperplasia Non-Herpetic Acute Limbic Encephalitis Obstructive Hydrocephalus Ocular Motor Apraxia Onchocerciasis Opsoclonus-Myoclonus Syndrome Optic Nerve Hypoplasia, Bilateral Oral Cavity Cancer Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to Orotic Aciduria Otitis Media Ovarian Cancer Pachygyria Pancreatic Cancer Pancreatitis Papilledema Paraganglioma Parametritis Paraplegia Parathyroid Carcinoma Paroxysmal Choreoathetosis Paroxysmal Nocturnal Hemoglobinuria Partial Third-Nerve Palsy Patent Ductus Venosus Pcdh19-Related Female-Limited Epilepsy Peeling Skin Syndrome 1 Peho-Like Syndrome Peho Syndrome Pellagra Pelvic Lipomatosis Pemphigus Pemphigus Vulgaris Peptic Ulcer Disease Pericarditis Peritonitis Periventricular Leukomalacia Pertussis Phaeochromocytoma Pheochromocytoma Photosensitive Epilepsy Pitt-Hopkins Syndrome Placental Insufficiency Plasmodium Falciparum Malaria Pneumonia Polyarteritis Nodosa Polymyositis Polyneuropathy Polyradiculoneuropathy Pontocerebellar Hypoplasia Pontocerebellar Hypoplasia, Type 4 Pontocerebellar Hypoplasia, Type 6 Porencephaly Porphyria Portal Hypertension Portal Vein Thrombosis Post-Traumatic Stress Disorder Postural Hypotension Post-Vaccinal Encephalitis Pre-Eclampsia Preeclampsia/eclampsia 1 Primary Biliary Cirrhosis Primary Central Nervous System Lymphoma Primary Cerebellar Degeneration Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type Primary Hepatic Neuroendocrine Carcinoma Prion Disease Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Progressive Multifocal Leukoencephalopathy Progressive Myoclonus Epilepsy Propionic Acidemia Prune Belly Syndrome Pseudobulbar Palsy Psychotic Disorder Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hypertension Purpura Pyle Disease Pyloric Stenosis Pyruvate Dehydrogenase E1-Alpha Deficiency Quadriplegia Recurrent Hypersomnia Renal Hypertension Renal Osteodystrophy Renal Tubular Acidosis Renovascular Hypertension Respiratory Syncytial Virus Infectious Disease Retinal Artery Occlusion Retinal Detachment Retinitis Retroperitoneal Fibrosis Rett Syndrome Reversible Cerebral Vasoconstriction Syndrome Reye Syndrome Rheumatoid Arthritis Ring Chromosome 20 Roberts Syndrome Rubella Salla Disease Salmonellosis Sarcoidosis 2 Sarcoma Schinzel Giedion Syndrome Schistosomiasis Schizoaffective Disorder Schizophrenia Scleromyxedema Scn2a Related Disorders Scn8a Encephalopathy Scn8a-Related Epilepsy with Encephalopathy Scorpion Envenomation Scrapie Segawa Syndrome, Autosomal Recessive Seizure Disorder Sensorineural Hearing Loss Serotonin Syndrome Severe Combined Immunodeficiency Severe Pre-Eclampsia Shigellosis Short Bowel Syndrome Sickle Cell Anemia Sickle Cell Disease Siderosis Sinusitis Sleeping Sickness Sneddon Syndrome Spastic Diplegia Spasticity Spastic Paraparesis Spinal Cord Injury Spinal Muscular Atrophy Spinocerebellar Degeneration Spiradenoma Spondyloocular Syndrome Spontaneous Intracranial Hypotension Sporadic Hemiplegic Migraine Sporadic Hyperekplexia Staphylococcal Toxic Shock Syndrome Status Epilepticus Stereotypic Movement Disorder Stxbp1 Encephalopathy with Epilepsy Subacute Delirium Subacute Thyroiditis Subcortical Arteriosclerotic Encephalopathy Succinic Semialdehyde Dehydrogenase Deficiency Sulfite Oxidase Deficiency, Isolated Superficial Siderosis Superior Mesenteric Artery Syndrome Susac Syndrome Symmetrical Thalamic Calcifications Synucleinopathy Systemic Lupus Erythematosus Systemic Mastocytosis Takayasu Arteritis T-Cell Leukemia Tetanus Tetraamelia Syndrome, Autosomal Recessive Thrombocytopenia Thrombophilia Thrombosis Thrombotic Thrombocytopenic Purpura Thunderclap Headache Thyroiditis Tic Disorder Tinea Capitis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tonsillitis Toxic Encephalopathy Toxic Shock Syndrome Toxoplasmoză Transient Global Amnesia Transitional Cell Carcinoma Transverse Myelitis Traumatic Brain Injury Tremor Trichinosis Tropical Spastic Paraparesis Trypanosomiasis Trypanosomiasis, Human East-African Tuberculous Meningitis Tuberous Sclerosis Typhoid Fever Urea Cycle Disorder Uremia Urogenital Tuberculosis Uterine Sarcoma Van Der Woude Syndrome 1 Vascular Dementia Vasculitis Viral Encephalitis Viral Hepatitis Wallerian Degeneration Weber Syndrome Wernicke Encephalopathy Wernicke-Korsakoff Syndrome West Syndrome Whiplash Williams-Beuren Syndrome Wilms Tumor 6 Wilson Disease Wolff-Parkinson-White Syndrome X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome Yemenite Deaf-Blind Hypopigmentation Syndrome Zinc-Responsive Necrolytic Acral Erythema
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