Informaţii despre

Nume Episodic Ataxia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Myotonic disorders
Clasificare anatomică Malacards Boli neuronale
Boli din aceeaşi familie Episodic Ataxia, Type 1; Episodic Ataxia, Type 2; Episodic Ataxia, Type 3; Episodic Ataxia, Type 4; Episodic Ataxia, Type 5; Episodic Ataxia, Type 6; Episodic Ataxia, Type 7; Episodic Ataxia, Type 8

Vezi şi

Boli A-Z Aging 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 Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Benign Familial Infantile Epilepsy Benign Familial Neonatal Epilepsy Benign Neonatal Seizures Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Central Nervous System Origin Vertigo Cerebritis Diarrhea Dicarboxylic Aminoaciduria Dyskinesia, Familial, with Facial Myokymia Dystonia Encephalitis Epilepsy Epilepsy, Familial Temporal Lobe, 3 Episodic Ataxia, Type 1 Episodic Ataxia, Type 2 Episodic Ataxia, Type 3 Episodic Ataxia, Type 4 Episodic Ataxia, Type 6 Episodic Ataxia, Type 7 Episodic Ataxia, Type 8 Erythromelalgia Familial Hemiplegic Migraine Familial or Sporadic Hemiplegic Migraine Glucose Transporter Type 1 Deficiency Syndrome Headache Hemiplegia Hemiplegic Migraine Hereditary Ataxia Laryngitis Malignant Hyperthermia Migraine with Aura Myoclonus Myotonic Dystrophy 2 Nervous System Disease Neuronitis Neuropathy Pharyngitis Pyruvate Kinase Deficiency of Red Cells Schizophrenia Scn2a Related Disorders Seizures, Benign Familial Infantile, 3 Seizures, Benign Familial Neonatal, 1 Somatization Disorder Spinocerebellar Ataxia 27 Spinocerebellar Ataxia 6 Spinocerebellar Ataxia Type 19/22 Spinocerebellar Atrophy Spondyloocular Syndrome Sporadic Hemiplegic Migraine Torticollis