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Boli A-Z Adolescence-Adult Electroclinical Syndrome Agenesis of the Corpus Callosum with Peripheral Neuropathy Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Apraxia Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 2 Bap1 Tumor Predisposition Syndrome Benign Epilepsy with Centrotemporal Spikes Benign Familial Infantile Epilepsy Benign Familial Neonatal Epilepsy Benign Neonatal Seizures Blepharospasm, Benign Essential Blood Group--Ahonen 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 Cdkl5-Related Disorder Cerebritis Childhood Absence Epilepsy Childhood Electroclinical Syndrome Chromosome 15q13.3 Deletion Syndrome Deafness, Autosomal Dominant 16 Early Myoclonic Encephalopathy Early Onset Absence Epilepsy Encephalopathy Epilepsy Epilepsy, Childhood Absence 1 Epilepsy, Idiopathic Generalized 10 Epilepsy, Idiopathic Generalized 2 Epilepsy, Idiopathic Generalized 3 Epilepsy, Idiopathic Generalized 4 Epilepsy, Idiopathic Generalized 5 Epilepsy, Idiopathic Generalized 7 Epilepsy, Juvenile Absence 1 Epilepsy, Myoclonic Juvenile Epilepsy, Nocturnal Frontal Lobe, 1 Epilepsy, Nocturnal Frontal Lobe, 3 Epilepsy with Generalized Tonic-Clonic Seizures Epileptic Encephalopathy, Early Infantile, 1 Epileptic Encephalopathy, Early Infantile, 15 Epileptic Encephalopathy, Early Infantile, 6 Epileptic Encephalopathy, Early Infantile, 9 Episodic Ataxia Episodic Ataxia, Type 1 Episodic Ataxia, Type 2 Episodic Ataxia, Type 7 Familial or Sporadic Hemiplegic Migraine Febrile Infection-Related Epilepsy Syndrome Febrile Seizures Focal Epilepsy Gaba-Transaminase Deficiency Generalized Epilepsy with Febrile Seizures Plus Generalized Epilepsy with Febrile Seizures Plus, Type 1 Genetic Epilepsy with Febrile Seizures Plus Glycine Encephalopathy Hemiplegia Hemiplegic Migraine Hepatic Adenomas, Familial Iminoglycinuria Immunoglobulin E Concentration, Serum Infancy Electroclinical Syndrome Infantile Epileptic Encephalopathy Jeavons Syndrome Juvenile Absence Epilepsy Lennox-Gastaut Syndrome Long Qt Syndrome Malaria, Mild Malignant Migrating Partial Seizures of Infancy Megaloblastic Anemia Megaloblastic Anemia 1 Mental Retardation, X-Linked, Syndromic, Hedera Type Myoclonic Astatic Epilepsy Myoclonic Epilepsy of Infancy Myoclonus Myoclonus Epilepsy Narcolepsy Neonatal Period Electroclinical Syndrome Neuronitis Obsessive-Compulsive Disorder Ocular Motor Apraxia Parametritis Perioral Myoclonia with Absences Schizophrenia Seizure Disorder Seizures, Benign Familial Infantile, 3 Seizures, Benign Familial Neonatal, 2 Spinocerebellar Ataxia 27 Spinocerebellar Ataxia 6 Sporadic Hemiplegic Migraine Status Epilepticus Stuttering Temporal Lobe Epilepsy Tobacco Addiction Unverricht-Lundborg Syndrome West Syndrome