Results: 1 to 20 of 466

Make selection to find tests for any of the checked conditions.[x]
ConditionsSynonyms
Epilepsy
  • Seizure Disorders
Epilepsy, idiopathic generalized, susceptibility to, 12
Epilepsy, idiopathic generalized 8
  • EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8
Epilepsy, idiopathic generalized 9
  • CACNB4-Related Juvenile Myoclonic Epilepsy
  • EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9
Epilepsy with grand mal seizures on awakening
  • CLCN2-Related Juvenile Myoclonic Epilepsy
  • EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11
Dentatorubral-pallidoluysian atrophy
  • Ataxia, chorea, seizures, and dementia
  • Haw River syndrome
  • Myoclonic epilepsy with choreoathetosis
  • Naito Oyanagi disease
Epilepsy, childhood absence 6
  • Epilepsy, Childhood Absence, Susceptibility to, 6
Unverricht-Lundborg syndrome
  • EPILEPSY, PROGRESSIVE MYOCLONIC, 1A
  • Epilepsy, progressive myoclonic type 1
  • Epilepsy, progressive myoclonus 1
  • Myoclonic epilepsy of Unverricht and Lundborg
  • Myoclonus progressive epilepsy of Unverricht and Lundborg
  • Progressive myoclonus epilepsy baltic myoclonic epilepsy
  • Unverricht-Lundborg Disease
Severe myoclonic epilepsy in infancy
  • Dravet syndrome
  • Epilepsy, Myoclonic, Infantile, Severe
  • Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)
  • GABRG2-Related Dravet Syndrome
  • SCN9A-Related Dravet Syndrome
Lafora disease
  • EPILEPSY, PROGRESSIVE MYOCLONIC, 2A
  • EPM2A-Related Lafora Disease
  • Epilepsy progressive myoclonic 2
  • Lafora body disorder
  • Myoclonic epilepsy of Lafora
  • NHLRC1-Related Lafora Disease
  • Progressive Myoclonus Epilepsy, Lafora Type
Epilepsy, juvenile myoclonic 5
  • EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13
  • EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 5
  • GABRA1-Related Juvenile Myoclonic Epilepsy
Benign familial neonatal seizures 1
  • Benign Neonatal Epilepsy 1
  • KCNQ2-Related Benign Familial Neonatal Epilepsy
Neuronal ceroid lipofuscinosis 8
  • CLN8 Disease
  • CLN8-Related Neuronal Ceroid-Lipofuscinosis
  • Northern epilepsy
Pyridoxine-dependent epilepsy
  • Pyridoxine dependency
  • Pyridoxine dependency with seizures
  • Pyridoxine-Dependent Seizures
  • Vitamin B6-dependent seizures
GLUT1 deficiency syndrome 2
  • Dystonia 18
  • GLUT1 deficiency syndrome 2, childhood onset
  • PAROXYSMAL EXERCISE-INDUCED DYSKINESIA WITH OR WITHOUT EPILEPSY AND/OR HEMOLYTIC ANEMIA
  • PAROXYSMAL EXERTION-INDUCED DYSTONIA WITH OR WITHOUT EPILEPSY AND/OR HEMOLYTIC ANEMIA
  • PED WITH OR WITHOUT EPILEPSY AND/OR HEMOLYTIC ANEMIA
  • Paroxysmal exercise-induced dystonia
  • Paroxysmal exertion-induced dyskinesia
  • PxMD-SLC2A1
Epilepsy, focal, with speech disorder and with or without mental retardation
  • APHASIA, ACQUIRED, WITH EPILEPSY
  • Acquired aphasia with convulsive disorder
  • Acquired epileptiform aphasia
  • Epilepsy with neurodevelopmental defects
  • GRIN2A-Related Disorders
  • Landau-Kleffner syndrome
  • Rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant
Epilepsy, idiopathic generalized 7
  • EIG7
  • EJM2-Related Juvenile Myoclonic Epilepsy
  • EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 7
Benign familial neonatal seizures 2
  • Benign Neonatal Epilepsy 2
  • CONVULSIONS, BENIGN FAMILIAL NEONATAL, 2
  • KCNQ3-Related Benign Familial Neonatal Epilepsy
  • KCNQ3-Related Disorders
Epilepsy, childhood absence 5
  • EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
Epilepsy, juvenile absence, susceptibility to, 1
  • Epilepsy, Absence

Results: 1 to 20 of 466

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