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Nume Myoclonus
Pagina Web www.malacards.org
Clasificari ICD10 Myoclonus
Clasificare anatomică Malacards Boli neuronale

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Boli A-Z 18p Deletion Syndrome Aceruloplasminemia Achalasia-Addisonianism-Alacrima Syndrome Acute Disseminated Encephalomyelitis Aging Aids Dementia Complex Alcohol Dependence Alexander Disease 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 Anaplastic Oligoastrocytoma Androgen Insensitivity Syndrome, Mild Angelman Syndrome Angiokeratoma Aniridia 1 Anorexia Nervosa 1 Anoxia Antiphospholipid Syndrome Arteriovenous Fistula Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Asthma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Autoimmune Autonomic Ganglionopathy Autoimmune Encephalitis Beckwith-Wiedemann Syndrome Benign Epilepsy with Centrotemporal Spikes Bickerstaff Brainstem Encephalitis Bleeding Disorder, Platelet-Type, 11 Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brain Ischemia Brainstem Auditory Evoked Responses Breast Cancer Brucellosis Bruxism Cardiac Arrest Celiac Disease 1 Central Nervous System Lymphoma Central Pontine Myelinolysis Cerebellar Astrocytoma Cerebral Hypoxia Cerebral Lipidosis Cerebral Palsy Cerebritis Cerebrotendinous Xanthomatosis Ceroid Lipofuscinosis, Neuronal, 6 Cervicitis Chikungunya Childhood Absence Epilepsy Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choroiditis Chromosomal Triplication Cluster Headache Coffin-Lowry Syndrome Communicating Hydrocephalus Cone-Rod Dystrophy 2 Congenital Generalized Lipodystrophy Cortical Blindness Corticobasal Degeneration Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniosynostosis with Fibular Aplasia Creutzfeldt-Jakob Disease Cystic Teratoma Cytochrome P450 2d6 Variant Dementia Dengue Virus Dentatorubral-Pallidoluysian Atrophy Diabetes Mellitus Dissociated Nystagmus Down Syndrome Dyskinetic Cerebral Palsy Dystonia Dystonia 11, Myoclonic Dystonia 15, Myoclonic Dystonia, Dopa-Responsive Encephalitis Encephalomyopathy Encephalopathy End Stage Renal Failure Eosinophilia-Myalgia Syndrome Epilepsy Epilepsy, Idiopathic Generalized 10 Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure Epilepsy, Progressive Myoclonic 7 Epileptic Encephalopathy, Early Infantile, 6 Episodic Ataxia Facial Hemiatrophy Febrile Seizures Fibrodysplasia Ossificans Progressiva Focal Epilepsy Focal Hand Dystonia Fragile X-Associated Tremor/ataxia Syndrome Fragile X Syndrome Frontotemporal Dementia Galactosialidosis Ganglioglioma Ganglioneuroblastoma Glioma Glucose Transporter Type 1 Deficiency Syndrome Glycogen Storage Disease Glycoproteinosis Good Syndrome Hashimoto's Encephalitis Headache Hemifacial Spasm Hemimegalencephaly Hepatitis Hepatitis C Hepatoblastoma Hereditary Ataxia Hereditary Neuropathies Hereditary Neuropathy with Liability to Pressure Palsy Hereditary Spastic Paraplegia Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypersomnia Hypertonia Hypertrophic Cardiomyopathy Hypertrophic Olivary Degeneration Hypogonadism Hypoxia Ichthyosis Infantile Epileptic Encephalopathy Influenza Internuclear Ophthalmoplegia Ischemia Japanese Encephalitis Krabbe Disease Lactic Acidosis Lambert-Eaton Myasthenic Syndrome Laryngitis Lateral Sclerosis Leber Hereditary Optic Neuropathy Leigh Syndrome Lennox-Gastaut Syndrome Limbic Encephalitis Lipid Storage Disease Lipodystrophy Lipomatosis Lissencephaly 1 Locked-in Syndrome Lung Cancer Lupus Erythematosus Lymphoma Lysosomal Storage Disease Machado-Joseph Disease Maple Syrup Urine Disease Mediastinitis Meningoencephalitis Mercury Poisoning Mitochondrial Complex Iii Deficiency Mitochondrial Disorders Mitochondrial Encephalomyopathy Mitochondrial Myopathy Moebius Syndrome Mood Disorder Moyamoya Disease 1 Mucolipidoses Multiple Sclerosis Multiple Symmetrical Lipomatosis Mumps Muscle Hypertrophy Muscular Atrophy Muscular Dystrophy Myasthenia Gravis Myelomeningocele Myoclonic Astatic Epilepsy Myoclonic Cerebellar Dyssynergia Myoclonic Epilepsy of Lafora Myoclonic Epilepsy of Unverricht and Lundborg Myoclonus and Ataxia Myoclonus Epilepsy Myoclonus, Familial Cortical Myopathy Myotonia Myotonic Dystrophy Nasopharyngitis Neuraminidase Deficiency Neuroblastoma Neurofibrosarcoma Neuroleptic Malignant Syndrome Neuromyelitis Optica Neuronal Ceroid-Lipofuscinoses Neuronitis Neuropathy Neuropathy, Hereditary, with Liability to Pressure Palsies Neurosyphilis Niemann-Pick Disease Obsessive-Compulsive Disorder Ocular Motor Apraxia Oligoastrocytoma Olivopontocerebellar Atrophy Opsoclonus-Myoclonus Syndrome Otitis Externa Pancreatitis Pandas Panencephalitis, Subacute Sclerosing Papilloma Paraneoplastic Syndromes Paraplegia Parasomnia, Sleep Bruxism Type Pellagra Periodic Limb Movement Disorder Peritonitis Pick Disease of Brain Pneumonia Polyneuropathy Pontine Hemorrhage Pontocerebellar Hypoplasia Porencephaly Postherpetic Neuralgia Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia Primary Central Nervous System Lymphoma Primary Cerebellar Degeneration Progressive Encephalomyelitis with Rigidity and Myoclonus Progressive Multifocal Leukoencephalopathy Progressive Muscular Atrophy Progressive Myoclonus Epilepsy Progressive Myoclonus Epilepsy, Lafora Type Propriospinal Myoclonus Prostate Cancer Prostatitis Pseudoxanthoma Elasticum Psychogenic Movement Pulmonary Tuberculosis Quadriplegia Rasmussen Encephalitis Reflex Epilepsy Reflex Sympathetic Dystrophy Restless Legs Syndrome Rett Syndrome Reunion Island Larsen Syndrome Reversible Cerebral Vasoconstriction Syndrome Riddle Syndrome Rubella Rubella Panencephalitis Salmonellosis Schizencephaly Schizophrenia Scn2a Related Disorders Scrub Typhus Segawa Syndrome, Autosomal Recessive Seizures, Benign Familial Neonatal, 1 Silver-Russell Syndrome Sleep Apnea Small Cell Carcinoma Spasmodic Dysphonia Spasmus Nutans Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Spastic Paraparesis Spastic Quadriplegia Spinal Cord Glioma Spinal Cord Injury Spinocerebellar Ataxia Type 16 Spinocerebellar Degeneration Spondyloocular Syndrome Spondylosis Startle Epilepsy Status Epilepticus Stiff-Person Syndrome Stuttering Syringomyelia Systemic Lupus Erythematosus Teratoma Thymoma Thyroiditis Tremor Trigeminal Neuralgia Unverricht-Lundborg Syndrome Vitamin B12 Deficiency West Nile Encephalitis West Nile Virus Xanthomatosis