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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
epilepsy +     
Myoclonus +     
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency  
Alopecia, Epilepsy, Pyorrhea, Mental Subnormality 
Alopecia-Epilepsy-Oligophrenia Syndrome of Moynahan 
Arthrogryposis Epileptic Seizures Migrational Brain Disorder 
autosomal dominant mental retardation 20  
Autosomal Dominant Mental Retardation 60  
autosomal recessive spinocerebellar ataxia 12  
Baraitser-Winter syndrome +   
Battaglia Neri Syndrome 
Beta-Amino Acids, Renal Transport of 
Borjeson-Forssman-Lehmann syndrome  
Boudhina Yedes Khiari syndrome 
branched-chain keto acid dehydrogenase kinase deficiency  
Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia 
Cerebellar Atrophy with Seizures and Variable Developmental Delay  
Christianson syndrome  
Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB 
Coffin Syndrome 1 
Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies  
Developmental Delay, Epilepsy, and Neonatal Diabetes  
Drug Resistant Epilepsy +   
early-onset vitamin B6-dependent epilepsy  
electroclinical syndrome +   
Epilepsy Telangiectasia 
EPILEPSY, EARLY-ONSET, WITH OR WITHOUT DEVELOPMENTAL DELAY  
Epilepsy, Hearing Loss, and Mental Retardation Syndrome  
Epilepsy, Occipital Calcifications 
Epilepsy, Post-Traumatic 
extratemporal epilepsy 
Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome  
Familial Convulsive Disorder with Prenatal or Early Onset 
Familial Myoclonus 1  
Familial Myoclonus 2  
Febrile Seizures +   
Feigenbaum Bergeron Richardson Syndrome 
Focal Cortical Dysplasia of Taylor +   
focal epilepsy +   
Generalized Epilepsy +   
Glycosylphosphatidylinositol Deficiency +   
Gurrieri Sammito Bellussi Syndrome 
Herrmann Syndrome 
Hot Water Epilepsy +  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES  
Intellectual Developmental Disorder with Behavioral Abnormalities and Craniofacial Dysmorphism with or without Seizures  
Intellectual Developmental Disorder with Macrocephaly, Seizures, and Speech Delay  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH POOR GROWTH AND WITH OR WITHOUT SEIZURES OR ATAXIA  
Intellectual Developmental Disorder with Seizures and Language Delay  
Kifafa Seizure Disorder 
Kohlschutter-Tonz syndrome  
Landau-Kleffner syndrome  
MEHMO syndrome  
Mental Retardation, Microcephaly, Epilepsy, and Coarse Face 
Microcephaly, Epilepsy, and Diabetes Syndrome  
Microcephaly, Growth Deficiency, Seizures, and Brain Malformations  
Myoclonic Epilepsies +   
A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic (i.e., occurring secondary to known disease processes such as infections, hypoxic-ischemic injuries, trauma, etc.).
Myoclonic Nystagmus 
Myoclonus, Cerebellar Ataxia, and Deafness 
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
Neonatal Intractable Myoclonus  
NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY  
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM  
Neurodevelopmental Disorder with Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination  
Neurodevelopmental Disorder with Epilepsy, Spasticity, and Brain Atrophy  
Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, EPILEPSY, AND GAIT ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND BRAIN ATROPHY  
NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT EARLY-ONSET GENERALIZED EPILEPSY  
Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech, and Seizures  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY  
Neurodevelopmental Disorder with Seizures and Nonepileptic Hyperkinetic Movements  
Neurodevelopmental Disorder with Seizures and Speech and Walking Impairment  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES  
Opsoclonus-Myoclonus Syndrome +   
PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES  
Photogenic Epilepsy with Spastic Diplegia and Mental Retardation 
Pitt-Hopkins syndrome +   
POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME  
Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy  
Progressive External Ophthalmoplegia with Myoclonus  
Progressive Microcephaly with Seizures and Cerebral and Cerebellar Atrophy  
Psychomotor Retardation, Epilepsy, and Craniofacial Dysmorphism  
pyridoxamine 5'-phosphate oxidase deficiency  
pyridoxine-dependent epilepsy  
Ramon Syndrome 
Retinal Degeneration and Epilepsy 
Rud Syndrome 
salt and pepper syndrome  
Sandhaus Ben-Ami Syndrome 
SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS  
SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  
Spinocerebellar Ataxia with Epilepsy  
status epilepticus +   
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
syndromic X-linked intellectual disability Hedera type  
visual epilepsy +   
Webb-Dattani Syndrome  
Wittwer Syndrome  
X-linked epilepsy with variable learning disabilities and behavior disorders  

Synonyms
Exact Synonyms: Cryptogenic Myoclonic Epilepsy ;   Epileptic seizures, myoclonic ;   Idiopathic Myoclonic Epilepsies ;   Idiopathic Myoclonic Epilepsy ;   Myoclonic Absence Epilepsies ;   Myoclonic Absence Epilepsy ;   Myoclonic Astatic Epilepsies ;   Myoclonic Astatic Epilepsy ;   Myoclonic Encephalopathies ;   Myoclonic Encephalopathy ;   Myoclonic Epilepsy ;   Myoclonic Seizure Disorder ;   Myoclonic Seizure Disorders ;   Myoclonic seizure ;   Myoclonic seizure disorder ;   Myoclonus Epilepsies ;   Myoclonus Epilepsy ;   cryptogenic myoclonic epilepsies ;   myoclonia epileptica ;   myoclonic epilepsy ;   symptomatic myoclonic epilepsies ;   symptomatic myoclonic epilepsy
Primary IDs: MESH:D004831
Alternate IDs: OMIA:002095
Definition Sources: MESH:D004831

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