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Nume Epilepsy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Epilepsy, unspecified
Clasificare anatomică Malacards Boli neuronale
Boli din aceeaşi familie Benign Familial Infantile Epilepsy

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Boli A-Z 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome Accommodative Spasm Aceruloplasminemia Achalasia Achalasia-Addisonianism-Alacrima Syndrome Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion Acute Lymphoblastic Leukemia, Childhood Acute Lymphocytic Leukemia Acute Mountain Sickness Acute Pancreatitis Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of Adams-Oliver Syndrome Adenoma Adenylosuccinase Deficiency Adie Pupil Adolescence-Adult Electroclinical Syndrome Agenesis of the Corpus Callosum with Peripheral Neuropathy Aging Agraphia Aicardi Syndrome Alacrima, Achalasia, and Mental Retardation Syndrome Alcohol Abuse Alcoholic Liver Cirrhosis Alexia Alexithymia Alobar Holoprosencephaly 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 Alternating Hemiplegia of Childhood Alzheimer Disease 3 Amelogenesis Imperfecta Aminoaciduria Amusia Amyotrophy, Monomelic Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Androgen Insensitivity Syndrome, Mild Aneurysm Angelman Syndrome Angiocentric Glioma Angiomatosis Anhaptoglobinemia Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Aortic Valve Disease 2 Aphasia Aplastic Anemia Apnea, Obstructive Sleep Apraxia Arachnoid Cysts Arachnoiditis Argininosuccinic Aciduria Aromatic L-Amino Acid Decarboxylase Deficiency Arterial Tortuosity Syndrome Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 2a Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Aspartylglucosaminuria Asperger Syndrome Asplenia, Isolated Congenital Asthma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Athetosis Atrial Fibrillation Atrioventricular Block Atrioventricular Septal Defect Attention Deficit-Hyperactivity Disorder Atypical Autism Audiogenic Seizures Autism Autism Spectrum Disorder Autoimmune Encephalitis Autoimmune Lymphoproliferative Syndrome Autonomic Dysfunction Autosomal Dominant Disease Autosomal Dominant Epilepsy with Auditory Features Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Autosomal Dominant Partial Epilepsy with Auditory Features Autosomal Recessive Cerebellar Ataxia Autosomal Recessive Disease Autosomal Recessive Nonsyndromic Deafness 86 Axenfeld-Rieger Syndrome Axonal Neuropathy Ayme-Gripp Syndrome Bacterial Meningitis Bainbridge-Ropers Syndrome Band Heterotopia Bap1 Tumor Predisposition Syndrome Baraitser-Winter Cerebrofrontofacial Syndrome Baraitser-Winter Syndrome 1 Basal Cell Carcinoma Basal Ganglia Calcification Behr Syndrome Benign Adult Familial Myoclonic Epilepsy Benign Childhood Occipital Epilepsy, Panayiotopoulos Type Benign Epilepsy with Centrotemporal Spikes Benign Familial Infantile Epilepsy Benign Familial Neonatal Epilepsy Benign Infantile Focal Epilepsy with Midline Spikes and Wave During Sleep Benign Neonatal Seizures Bilateral Frontal Polymicrogyria Biotinidase Deficiency Bipolar Disorder Bipolar I Disorder Bleeding Disorder, Platelet-Type, 11 Blepharophimosis Blepharospasm, Benign Essential Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System 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 Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Borna Disease Brain Cancer Brain Injury Brain Ischemia Branchiootic Syndrome 1 Breast Cancer Brugada Syndrome Burns Capgras Syndrome Capillary Malformations, Congenital Cardiac Arrhythmia Cataract Catecholaminergic Polymorphic Ventricular Tachycardia Cavernous Hemangioma Cavernous Malformation Cdkl5-Related Disorder Celiac Disease 1 Cellulitis Central Nervous System Disease Central Nervous System Origin Vertigo Centralopathic Epilepsy Central Precocious Puberty Central Sleep Apnea Cerebellar Astrocytoma Cerebellar Atrophy, Developmental Delay, and Seizures Cerebellar Hypoplasia Cerebral Aneurysms Cerebral Artery Occlusion Cerebral Atrophy Cerebral Cavernous Malformations Cerebral Creatine Deficiency Syndrome 1 Cerebral Degeneration Cerebral Hypoxia Cerebral Palsy Cerebritis Cerebrotendinous Xanthomatosis Cerebrovascular Disease Ceroid Lipofuscinosis, Neuronal, 13 Ceroid Lipofuscinosis, Neuronal, 6 Ceroid Lipofuscinosis, Neuronal, 8, Northern Epilepsy Variant Charcot-Marie-Tooth Disease Charles Bonnet Syndrome Cherubism Childhood Absence Epilepsy Childhood Electroclinical Syndrome Cholestasis-Lymphedema Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choreoacanthocytosis Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Chorioretinitis Choroiditis Chromosomal Triplication Chromosome 12p Duplication Chromosome 15q11.2 Deletion Syndrome Chromosome 15q13.3 Deletion Syndrome Chromosome 15q Deletion Chromosome 1p36 Deletion Syndrome Chromosome 22q11.2 Duplication Syndrome Chromosome Xp Deletion Chromosome Xq Deletion Clark-Baraitser Syndrome Cleft Larynx, Posterior Cleidocranial Dysplasia Spectrum Disorder Cocaine Abuse Coffin-Lowry Syndrome Cognitive Function 1, Social Cohen-Gibson Syndrome Colpocephaly Complex Partial Epilepsy Congenital Cytomegalovirus Congenital Disorders of N-Linked Glycosylation and Multiple Pathway Congenital Generalized Lipodystrophy Congenital Toxoplasmosis Conversion Disorder Coproporphyria, Hereditary Corneal Dystrophy, Fleck Corneal Dystrophy, Meesmann Cornelia De Lange Syndrome Cortical Blindness Cortical Dysplasia, Complex, with Other Brain Malformations 7 Coumarin Resistance Cranial Nerve Palsy Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniopharyngioma Craniosynostosis Creutzfeldt-Jakob Disease Cri-Du-Chat Syndrome Crouzon Syndrome Crouzon Syndrome with Acanthosis Nigricans Cutis Laxa Cutis Verticis Gyrata Cutis Verticis Gyrata Mental Deficiency Cyclic Vomiting Syndrome Cystic Adenomatoid Malformation of Lung Cysticercosis Cystitis Cytochrome P450 2d6 Variant Cytomegalovirus Infection Dandy-Walker Syndrome Delusional Disorder Dementia Dental Caries Dentatorubral-Pallidoluysian Atrophy Depdc5-Related Epilepsy Developmental Coordination Disorder Diabetes Mellitus Diabetes Mellitus, Permanent Neonatal Diencephalic Syndrome Digeorge Syndrome Dihydropyrimidine Dehydrogenase Deficiency Dilated Cardiomyopathy Diphtheria Dissociative Disorder Dissociative Seizures Down Syndrome Drug Dependence Drug Rash with Eosinophilia and Systemic Symptoms Duane Retraction Syndrome 1 Dwarfism Dysautonomia Dyscalculia Dysembryoplastic Neuroepithelial Tumor Dysgraphia Dyskeratosis Congenita, X-Linked Dyskinetic Cerebral Palsy Dyslexia Dysostosis Dystonia Early Myoclonic Encephalopathy Early Onset Absence Epilepsy Eating Disorder Eating Reflex Epilepsy Echolalia Eclampsia Ectopic Pregnancy Ehlers-Danlos Syndrome Encephalitis Encephalocele Encephalocraniocutaneous Lipomatosis Encephalomalacia Encephalomyopathy Encephalopathy Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Endotheliitis Ependymoma Epilepsy-Aphasia Spectrum Epilepsy, Childhood Absence 1 Epilepsy, Familial Adult Myoclonic, 2 Epilepsy, Familial Adult Myoclonic, 3 Epilepsy, Familial Focal, with Variable Foci 1 Epilepsy, Familial Temporal Lobe, 3 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation Epilepsy, Idiopathic Generalized Epilepsy, Idiopathic Generalized 10 Epilepsy, Idiopathic Generalized 7 Epilepsy, Juvenile Absence 1 Epilepsy, Myoclonic Juvenile Epilepsy, Nocturnal Frontal Lobe, 1 Epilepsy, Nocturnal Frontal Lobe, 3 Epilepsy, Nocturnal Frontal Lobe, 4 Epilepsy, Partial, with Pericentral Spikes Epilepsy, Progressive Myoclonic, 1b Epilepsy, Progressive Myoclonic 7 Epilepsy, Pyridoxine-Dependent Epilepsy with Generalized Tonic-Clonic Seizures Epilepsy with Myoclonic Absences Epileptic Encephalopathy, Early Infantile, 1 Epileptic Encephalopathy, Early Infantile, 15 Epileptic Encephalopathy, Early Infantile, 16 Epileptic Encephalopathy, Early Infantile, 3 Epileptic Encephalopathy, Early Infantile, 36 Epileptic Encephalopathy, Early Infantile, 39 Epileptic Encephalopathy, Early Infantile, 4 Epileptic Encephalopathy, Early Infantile, 6 Epileptic Encephalopathy, Early Infantile, 7 Episodic Ataxia Episodic Ataxia, Type 1 Episodic Ataxia, Type 2 Esotropia Essential Tremor Euthyroid Sick Syndrome Extratemporal Epilepsy Extraventricular Neurocytoma Facial Hemiatrophy Factor Vii Deficiency Factor Xiii Deficiency Fainting Familial Hemiplegic Migraine Fanconi Anemia, Complementation Group E Fanconi Syndrome Febrile Infection-Related Epilepsy Syndrome Febrile Seizures Febrile Seizures, Familial, 1 Febrile Seizures, Familial, 11 Febrile Seizures, Familial, 4 Fetishism Fibromatosis Focal Cortical Dysplasia, Type Ii Focal Dermal Hypoplasia Focal Dystonia Focal Epilepsy Foix Chavany Marie Syndrome Folinic Acid-Responsive Seizures Foxg1 Syndrome Fragile X Syndrome Galactose Epimerase Deficiency Galloway-Mowat Syndrome Gangliocytoma Ganglioglioma Gastroenteritis Generalized Anxiety Disorder Generalized Epilepsy with Febrile Seizures Plus Generalized Epilepsy with Febrile Seizures Plus, Type 1 Generalized Epilepsy with Febrile Seizures Plus, Type 2 Genetic Epilepsy with Febrile Seizures Plus Genetic Reflex Epilepsy Genitopatellar Syndrome Gilles De La Tourette Syndrome Gingival Fibromatosis Gingival Overgrowth Gingivitis Glioblastoma Glioblastoma Multiforme Glioma Gliomatosis Cerebri Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glomerulonephritis Glucose Transporter Type 1 Deficiency Syndrome Glutaric Acidemia I Glycogen Storage Disease Glycosylphosphatidylinositol Biosynthesis Defect 15 Goldberg-Shprintzen Syndrome Gout Graves' Disease Grin2a-Related Speech Disorders and Epilepsy Growth Hormone Deficiency Gurrieri Syndrome Haemophilus Influenzae Haim-Munk Syndrome Hartsfield Syndrome Headache Head Injury Helix Syndrome Hemangioma Hemifacial Atrophy, Progressive Hemifacial Spasm Hemihyperplasia, Isolated Hemimegalencephaly Hemiplegia Hemiplegic Migraine Hemochromatosis, Type 1 Hemosiderosis Hepatic Adenomas, Familial Hepatic Coma Hepatitis Hereditary Spastic Paraplegia Herpes Simplex Herpes Simplex Encephalitis High Pressure Neurological Syndrome Hinman Syndrome Holoprosencephaly Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Hydrocephalus Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperandrogenism Hypercholesterolemia, Autosomal Dominant, 3 Hypercoagulability Syndrome Due to Glycosylphosphatidylinositol Deficiency Hyperekplexia Hyperglycemia Hyperinsulinemic Hypoglycemia, Familial, 6 Hyperinsulinism Hyperprolinemia Hypersomnia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hyperthyroidism Hypertrichosis Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypocalcemia, Autosomal Dominant 1 Hypochondroplasia Hypoglycemia Hypogonadism Hypomelanosis of Ito Hypoparathyroidism Hypopituitarism Hypothalamic Hamartomas Hypotonia Hypotrichosis 1 Hypoxia Ichthyosis Ichthyosis, Congenital, Autosomal Recessive 11 Idiopathic Hemiconvulsion-Hemiplegia Syndrome Immunoglobulin E Concentration, Serum Impulse Control Disorder Infancy Electroclinical Syndrome Infantile Epileptic Encephalopathy Infertility Inflammatory Linear Verrucous Epidermal Nevus Influenza Inherited Metabolic Disorder Insulinoma Intervertebral Disc Disease Intracranial Aneurysm Iqsec2 Ischemia Isolated Optic Neuritis Jeavons Syndrome Jumping Frenchmen of Maine Juvenile Absence Epilepsy Juvenile Rheumatoid Arthritis Kabuki Syndrome 1 Keratoconus Kleptomania Kluver-Bucy Syndrome Knobloch Syndrome Kohlschutter-Tonz Syndrome L-2-Hydroxyglutaric Aciduria Lactic Acidosis Landau-Kleffner Syndrome Lateral Sclerosis Learning Disability Leigh Syndrome Lennox-Gastaut Syndrome Leukemia Leukodystrophy Leukomalacia Limb-Girdle Muscular Dystrophy Limbic Encephalitis Linear Scleroderma Lipodystrophy Lipoic Acid Synthetase Deficiency Lipoid Proteinosis of Urbach and Wiethe Lipomatosis Lissencephaly Lissencephaly 1 Liver Cirrhosis Long Qt Syndrome Lubs X-Linked Mental Retardation Syndrome Lupus Erythematosus Lymphatic Malformations Lymphoblastic Leukemia Lymphoma Lymphoproliferative Syndrome Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Macrocytic Anemia Macroglossia Macs Syndrome Macular Dystrophy, Corneal Malaria Malaria, Mild Malignant Migrating Partial Seizures of Infancy Mannosidosis Mast Cell Activation Syndrome Mbd5 Haploinsufficiency Mccune-Albright Syndrome Medullary Sponge Kidney Megacolon Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 Megalencephaly Megaloblastic Anemia Megalocornea Melnick-Needles Syndrome Meningioma, Familial Meningitis Meningoencephalocele Menkes Disease Mental Retardation, X-Linked, Syndromic, Hedera Type Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis Metabolic Acidosis Metachromatic Leukodystrophy Metaphyseal Dysplasia, Spahr Type Microcephaly Microcephaly, Epilepsy, and Diabetes Syndrome Microcephaly with Simplified Gyral Pattern Migraine, Familial Hemiplegic, 2 Migraine with Aura Migraine with or Without Aura 2 Mitochondrial Complex I Deficiency Mitochondrial Disorders Mitochondrial Encephalomyopathy Mitochondrial Myopathy Miyoshi Muscular Dystrophy 1 Mohr-Tranebjaerg Syndrome Molybdenum Cofactor Deficiency Monosomy 22 Monosomy 7 of Bone Marrow Mood Disorder Mosaic Variegated Aneuploidy Syndrome 1 Motor Neuron Disease Mowat-Wilson Syndrome Moyamoya Disease 1 Mucolipidosis Iv Mucopolysaccharidosis, Type Vii Muenke Syndrome Muir-Torre Syndrome Multiple Acyl-Coa Dehydrogenase Deficiency Multiple Chemical Sensitivity Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Multiple Endocrine Neoplasia Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple Symmetrical Lipomatosis Murcs Association Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Duchenne and Becker Type Muscular Dystrophy, Duchenne Type Muscular Dystrophy-Dystroglycanopathy Mutism Myelitis Myelomeningocele Myocardial Infarction Myocardial Stunning Myoclonic-Astastic Epilepsy Myoclonic Astatic Epilepsy Myoclonic-Atonic Epilepsy Myoclonic Epilepsy Associated with Ragged-Red Fibers Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders Myoclonic Epilepsy, Familial Infantile Myoclonic Epilepsy of Infancy Myoclonic Epilepsy of Lafora Myoclonic Epilepsy of Unverricht and Lundborg Myoclonus Myoclonus Epilepsy Myopathy Myotonia Myotonic Dystrophy Myxopapillary Ependymoma Narcolepsy Neonatal Diabetes Mellitus Neonatal Period Electroclinical Syndrome Nephronophthisis Nephrotic Syndrome Nervous System Disease Neuroaxonal Dystrophy Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuroleptic Malignant Syndrome Neuromuscular Disease Neuromyelitis Optica Neuromyelitis Optica Spectrum Disorder Neuronal Ceroid-Lipofuscinoses Neuronal Ceroid Lipofuscinosis Neuronal Migration Disorders Neuronitis Neuropathy Neurosarcoidosis Neurosyphilis Neutropenia Nicolaides-Baraitser Syndrome Niemann-Pick Disease Niemann-Pick Disease, Type a Night Blindness Nipples Inverted Nodding Syndrome Nonsyndromic Deafness Normokalemic Periodic Paralysis Norrie Disease Norse Obsessive-Compulsive Disorder Obstructive Hydrocephalus Ocular Motor Apraxia Oligoastrocytoma Oligodendroglioma Oliver Syndrome Onchocerciasis Optic Nerve Hypoplasia, Bilateral Orbital Cellulitis Orotic Aciduria Osteopetrosis Pachygyria Paine Syndrome Pallister-Hall Syndrome Pancreatitis Panic Disorder Papilloma Parametritis Paranoid Schizophrenia Paraplegia Paraquat Poisoning Paroxysmal Choreoathetosis Partial Motor Epilepsy Patau Syndrome Pathological Gambling Pcdh19-Related Female-Limited Epilepsy Pediatric Arterial Ischemic Stroke Peeling Skin Syndrome 1 Peho Syndrome Pemphigus Pemphigus Vulgaris Periodic Limb Movement Disorder Periodontal Disease Periodontitis Perioral Myoclonia with Absences Periventricular Leukomalacia Periventricular Nodular Heterotopia Peroxisome Disorders Personality Disorder Pertussis Pervasive Developmental Disorder Pharyngitis Phelan-Mcdermid Syndrome Phenylketonuria Phonagnosia Phosphoglycerate Dehydrogenase Deficiency Photoparoxysmal Response 1 Photosensitive Epilepsy Pick Disease of Brain Pilocytic Astrocytoma Pineal Cyst Pituitary Adenoma Pleomorphic Xanthoastrocytoma Polydactyly Polyhydramnios Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy Polykaryocytosis Inducer Polymicrogyria Polyneuropathy Pontocerebellar Hypoplasia Pontocerebellar Hypoplasia, Type 3 Porencephaly Porphyria Porphyria Cutanea Tarda Posterior Cortical Atrophy Postpartum Depression Posttransplant Acute Limbic Encephalitis Post-Traumatic Epilepsy Post-Traumatic Stress Disorder Postural Orthostatic Tachycardia Syndrome Prader-Willi Syndrome Precocious Puberty Pre-Eclampsia Premature Ovarian Failure 7 Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia Primary Ciliary Dyskinesia Primary Familial Brain Calcification Progressive Myoclonus Epilepsy Progressive Myoclonus Epilepsy, Lafora Type Propionic Acidemia Protein S Deficiency Protoplasmic Astrocytoma Pseudobulbar Palsy Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ia Psychotic Disorder Ptosis Pulmonary Alveolar Microlithiasis Pulmonary Edema Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pure Red-Cell Aplasia Pyle Disease Pyridoxal 5'-Phosphate-Dependent Epilepsy Quadriplegia Rabies Ramon Syndrome Rasmussen Encephalitis Reading Disorder Recurrent Hypersomnia Reflex Epilepsy Resting Heart Rate, Variation in Restless Legs Syndrome Retinal Degeneration Retinitis Retinitis Pigmentosa Rett Syndrome Rheumatic Disease Rheumatoid Arthritis Rhombencephalosynapsis Ring Chromosome 14 Syndrome Ring Chromosome 17 Ring Chromosome 18 Ring Chromosome 19 Ring Chromosome 20 Ring Chromosome 4 Rolandic Epilepsy-Speech Dyspraxia Syndrome Rud Syndrome Salt and Pepper Developmental Regression Syndrome Satb2-Associated Syndrome Scapuloperoneal Myopathy, X-Linked Dominant Schizencephaly Schizophrenia Scn2a Related Disorders Scn8a Encephalopathy Scn8a-Related Epilepsy with Encephalopathy Second-Degree Atrioventricular Block Seizure Disorder Seizures, Benign Familial Infantile, 3 Seizures, Benign Familial Neonatal, 1 Seizures, Benign Familial Neonatal, 2 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance Severe Congenital Neutropenia Severe Cutaneous Adverse Reaction Shaken Baby Syndrome Shapiro Syndrome Sick Sinus Syndrome Siderosis Simple Partial Epilepsy Sinusitis Skeletal Dysplasias Skin Disease Sleep Apnea Sleep Disorder Smith-Magenis Syndrome Sotos Syndrome 1 Sparganosis Spastic Ataxia, Charlevoix-Saguenay Type Spastic Cerebral Palsy Spastic Hemiplegia Spasticity Spastic Paraparesis Spastic Quadriplegia Speech Disorder Spinal Arachnoiditis Spinal Meningioma Spinal Muscular Atrophy Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy Spinocerebellar Ataxia Type 19/22 Spiradenoma Split-Hand/foot Malformation 1 Spondyloocular Syndrome Sporadic Hemiplegic Migraine Startle Epilepsy Status Epilepticus Stereotypic Movement Disorder Stickler Syndrome Stiff-Person Syndrome Strabismus Striatal Degeneration, Autosomal Dominant 2 Sturge-Weber Syndrome Stuttering Stxbp1 Encephalopathy with Epilepsy Subcortical Band Heterotopia Subependymal Giant Cell Astrocytoma Subependymal Nodular Heterotopia Succinic Semialdehyde Dehydrogenase Deficiency Superficial Siderosis Syncope Syndrome of Inappropriate Antidiuretic Hormone Syndromic Intellectual Disability Systemic Lupus Erythematosus Taeniasis Temple-Baraitser Syndrome Temporal Lobe Epilepsy Tetanus Tetralogy of Fallot Thalamic Neoplasm Three M Syndrome 1 Thyroiditis Tic Disorder Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tooth Disease Toxocariasis Toxoplasmoză Transient Global Amnesia Transverse Myelitis Transvestism Traumatic Brain Injury Treacher Collins Syndrome 1 Tremor Trimethylaminuria Trisomy 22 Tuberculous Meningitis Tuberous Sclerosis Turner Syndrome Unilateral Polymicrogyria Unverricht-Lundborg Syndrome Vasculitis Velocardiofacial Syndrome Ventricular Septal Defect Viral Encephalitis Visual Epilepsy Weber Syndrome West Syndrome Williams-Beuren Syndrome Wilson Disease Wolff-Parkinson-White Syndrome Wolf-Hirschhorn Syndrome Xanthomatosis X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome X-Linked Lissencephaly with Abnormal Genitalia Zika Virus Infection
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