Informaţii despre

Nume Seizures, Benign Familial Neonatal, 1
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli neuronale
Boli din aceeaşi familie Seizures Benign Familial Neonatal Recessive Form; Seizures, Benign Familial Neonatal, 2; Seizures, Benign Familial Neonatal, 3; Seizures, Benign Familial Neonatal, Autosomal Recessive

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Boli A-Z Aging 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 Aniridia 1 Anorexia Nervosa 1 Arachnoid Cysts Arachnoiditis Arteriovenous Fistula Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Behr Syndrome Bell's Palsy Benign Neonatal Seizures Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Brain Stem Cancer Brain Stem Glioma Brown's Tendon Sheath Syndrome Cervicitis Charcot-Marie-Tooth Disease Chronic Inflammatory Demyelinating Polyradiculoneuropathy Communicating Hydrocephalus Congenital Smooth Muscle Hamartoma Convulsions Benign Familial Neonatal Dominant Form Demyelinating Disease Dermatomyositis Dyskinesia, Familial, with Facial Myokymia Dystonia Encephalopathy Eosinophilia-Myalgia Syndrome Epilepsy Episodic Ataxia Glioma Hansen's Disease Hemifacial Spasm Hepatitis Hepatitis B Hereditary Ataxia Hereditary Spastic Paraplegia Hydrocephalus Hypoglycemia Isolated Facial Myokymia Laryngitis Lateral Sclerosis Linear Scleroderma Medulloblastoma Melanoma Motor Neuron Disease Mucoepidermoid Carcinoma Multiple Sclerosis Multiple System Atrophy 1 Muscle Hypertrophy Myoclonus Myokymia with Neonatal Epilepsy Myotonia Nasopharyngeal Carcinoma Nasopharyngitis Neuronitis Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iia Neurosarcoidosis Ocular Motility Disease Ocular Neuromyotonia Paine Syndrome Paraplegia Peripheral Nervous System Disease Plexopathy Polyneuropathy Polyradiculoneuropathy Ptosis Retinitis Retinitis Pigmentosa Scoliosis Seizures, Benign Familial Infantile, 1 Seizures, Benign Familial Infantile, 3 Seizures, Benign Familial Neonatal, 2 Seizures, Benign Familial Neonatal, 3 Seizures, Benign Familial Neonatal, Autosomal Recessive Seizures Benign Familial Neonatal Recessive Form Spasticity Spastic Paraparesis Spinal Stenosis Syringobulbia Teratoma Thymoma Thyroiditis Tooth Disease Tremor Visual Epilepsy X-Linked Charcot-Marie-Tooth Disease