Informaţii despre

Nume Seizure Disorder
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli neuronale
Boli din aceeaşi familie Seizures, Benign Familial Infantile, 1; Seizures, Benign Familial Infantile, 2; Seizures, Benign Familial Infantile, 3; Seizures, Benign Familial Infantile, 4; Seizures, Benign Familial Infantile, 5

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Boli A-Z Adie Pupil Aging Agoraphobia Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aneurysm Angelman Syndrome Aniridia 1 Anorexia Nervosa 1 Aphasia Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Attention Deficit-Hyperactivity Disorder Autism Autism Spectrum Disorder Ayme-Gripp Syndrome Behr Syndrome Benign Familial Infantile Epilepsy Benign Familial Neonatal Epilepsy Benign Neonatal Seizures Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brain Injury Bruxism Cataract Cdkl5-Related Disorder Cerebral Aneurysms Cerebritis Choreatic Disease Cleft Lip Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cutaneous Solitary Mastocytoma Cysticercosis Down Syndrome Dystonia, Dopa-Responsive Early Myoclonic Encephalopathy Early Onset Absence Epilepsy Eclampsia Encephalitis Encephalocele Encephalomalacia Encephalopathy Epilepsy Epilepsy, Familial Temporal Lobe, 3 Epilepsy, Nocturnal Frontal Lobe, 1 Epilepsy with Generalized Tonic-Clonic Seizures Epileptic Encephalopathy, Early Infantile, 15 Epileptic Encephalopathy, Early Infantile, 6 Epileptic Encephalopathy, Early Infantile, 9 Extracutaneous Mastocytoma Familial Hemiplegic Migraine Familial or Sporadic Hemiplegic Migraine Febrile Seizures Fetal Alcohol Syndrome Gait Apraxia Gastroesophageal Reflux Generalized Epilepsy with Febrile Seizures Plus Germ Cells Tumors Glioma Glut1 Deficiency Syndrome 2 Head Injury Hemiplegia Hemiplegic Migraine Hepatic Adenomas, Familial Hepatitis Herpes Simplex Hinman Syndrome Hydrocephalus Hydrocephalus, Nonsyndromic, Autosomal Recessive 1 Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 Hyperprolactinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoglycemia Hypoparathyroidism Hypotonia Infancy Electroclinical Syndrome Infantile Epileptic Encephalopathy Infantile Hypotonia Infertility Insulinoma Japanese Encephalitis Kifafa Seizure Disorder Lennox-Gastaut Syndrome Long Qt Syndrome Malignant Hypertension Malignant Migrating Partial Seizures of Infancy Mechanical Strabismus Meningitis Microcephaly Muscular Dystrophy Myoclonic Astatic Epilepsy Neonatal Period Electroclinical Syndrome Neuronitis Neurosyphilis Nonseminomatous Germ Cell Tumor Obsessive-Compulsive Disorder Orofacial Cleft Osteomalacia Panic Disorder Paroxysmal Choreoathetosis Pituitary Hormone Deficiency, Combined, 2 Prader-Willi Syndrome Pseudohypoparathyroidism Psychotic Disorder Respiratory Syncytial Virus Infectious Disease Rett Syndrome Ring Chromosome 20 Schimke Immunoosseous Dysplasia Schizophrenia Scn1a-Related Seizure Disorders Seizures, Benign Familial Infantile, 3 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Slipped Capital Femoral Epiphysis Spondyloocular Syndrome Strabismus Sturge-Weber Syndrome Substance Abuse Syncope Syndromic Intellectual Disability Temporal Lobe Epilepsy Tetanus Tetralogy of Fallot Thrombosis Visual Epilepsy Weber Syndrome West Syndrome Wolf-Hirschhorn Syndrome