Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency  
Alopecia, Epilepsy, Pyorrhea, Mental Subnormality 
Alopecia-Epilepsy-Oligophrenia Syndrome of Moynahan 
Amniotic Band Syndrome +  
Arthrogryposis Epileptic Seizures Migrational Brain Disorder 
asphyxia neonatorum +   
autosomal dominant mental retardation 20  
Autosomal Dominant Mental Retardation 60  
autosomal recessive spinocerebellar ataxia 12  
Baraitser-Winter syndrome +   
Battaglia Neri Syndrome 
benign familial neonatal epilepsy +   
benign neonatal seizures +   
A condition marked by recurrent seizures that occur during the first 4-6 weeks of life despite an otherwise benign neonatal course. Autosomal dominant familial and sporadic forms have been identified. Seizures generally consist of brief episodes of tonic posturing and other movements, apnea, eye deviations, and blood pressure fluctuations. These tend to remit after the 6th week of life. The risk of developing epilepsy at an older age is moderately increased in the familial form of this disorder. (Neurologia 1996 Feb;11(2):51-5)
Beta-Amino Acids, Renal Transport of 
Birth Injuries +   
Borjeson-Forssman-Lehmann syndrome  
Boudhina Yedes Khiari syndrome 
branched-chain keto acid dehydrogenase kinase deficiency  
Caffey disease +   
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
Cerebellar Atrophy with Seizures and Variable Developmental Delay  
Christianson syndrome  
Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB 
Coffin Syndrome 1 
Colic 
Congenital Hyperinsulinism +   
Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies  
congenital nystagmus +   
congenital syphilis +  
congenital toxoplasmosis 
Cutis Laxa-Marfanoid Syndrome 
cystic fibrosis +   
Developmental Delay, Epilepsy, and Neonatal Diabetes  
Drug Resistant Epilepsy +   
early infantile epileptic encephalopathy +   
early myoclonic encephalopathy +   
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  
Febrile Seizures +   
fetal erythroblastosis +   
Focal Cortical Dysplasia of Taylor +   
focal epilepsy +   
Generalized Epilepsy +   
Glycosylphosphatidylinositol Deficiency +   
Gurrieri Sammito Bellussi Syndrome 
Hot Water Epilepsy +  
hydrophthalmos +   
Hyperglycinemia, Transient Neonatal 
Hyperparathyroidism, Neonatal Severe Primary  
ichthyosis +   
Infantile Hypercalcemia +   
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  
meconium aspiration syndrome  
Meconium Ileus  
MEHMO syndrome  
Mental Retardation, Microcephaly, Epilepsy, and Coarse Face 
Microcephaly, Epilepsy, and Diabetes Syndrome  
Microcephaly, Growth Deficiency, Seizures, and Brain Malformations  
Mobius syndrome +   
Myoclonic Epilepsies +   
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
neonatal abstinence syndrome 
Neonatal Alloimmune Thrombocytopenia  
neonatal anemia +   
neonatal diabetes +   
Neonatal Hyperbilirubinemia +   
Neonatal Hypoglycemia, Simulating Foetopathia Diabetica  
Neonatal Inflammatory Skin and Bowel Disease +   
Neonatal Pulmonary Hypertension  
Neonatal Sepsis  
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, Autosomal Dominant  
NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES  
Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech, and Seizures  
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  
ophthalmia neonatorum 
PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES  
persistent fetal circulation syndrome  
Photogenic Epilepsy with Spastic Diplegia and Mental Retardation 
Pitt-Hopkins syndrome +   
POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME  
Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy  
Posttransfusion Purpura  
Premature Infant Diseases +   
Psychomotor Retardation, Epilepsy, and Craniofacial Dysmorphism  
pyridoxamine 5'-phosphate oxidase deficiency  
pyridoxine-dependent epilepsy  
Ramon Syndrome 
Retinal Degeneration and Epilepsy 
Rothmund-Thomson syndrome +   
Rud Syndrome 
salt and pepper syndrome  
Sandhaus Ben-Ami Syndrome 
Sclerema Neonatorum 
SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS  
SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  
severe combined immunodeficiency +   
Spinocerebellar Ataxia with Epilepsy  
status epilepticus +   
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
syndromic X-linked intellectual disability Hedera type  
thanatophoric dysplasia +   
transient neonatal thrombocytopenia 
umbilical hernia +   
visual epilepsy +   
vitamin K deficiency bleeding  
Webb-Dattani Syndrome  
Wittwer Syndrome  
Wolman disease +   
X-linked epilepsy with variable learning disabilities and behavior disorders  

Synonyms
Exact Synonyms: Benign Neonatal Convulsion ;   Benign Neonatal Convulsions ;   Benign Neonatal Epilepsies ;   Benign Neonatal Non Familial Convulsions ;   Benign Neonatal-Infantile Epilepsies ;   Benign Neonatal-Infantile Epilepsy ;   NEONATAL SEIZURES ;   benign neonatal epilepsy ;   benign neonatal nonfamilial epilepsy ;   non familial benign neonatal epilepsy
Primary IDs: MESH:D020936
Alternate IDs: RDO:0000537
Xrefs: NCI:C84593 ;   OMIM:PS121200 ;   ORDO:1949
Definition Sources: http://en.wikipedia.org/wiki/Benign_familial_neonatal_epilepsy "DO", http://www.ncbi.nlm.nih.gov/books/NBK32534/ "DO", http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=140927 "DO", MESH:D020936

paths to the root