Disease Browser
Parent Node: Epilepsy (D004827) Parent Node: Infant, Newborn, Diseases (D007232) ..Starting node .. Epilepsy, Benign Neonatal (D020936) Child Nodes:
........Convulsions benign familial neonatal dominant form (C535466) ........Convulsions, Benign Familial Infantile, 4 (C567231) ........Convulsions, Benign Familial Neonatal, 1, And/Or Myokymia (C567744) ........Convulsions, Benign Familial Neonatal, 1, Atypical Severe (C567746) ........Epilepsy, Benign Neonatal, 1 (C565164) ........Epilepsy, Benign Neonatal, 1, Atypical Severe (C567745) ........Epilepsy, Benign Neonatal, 3 (C564274) ........Epilepsy, Benign Neonatal, Autosomal Recessive (C564823) ........Infantile convulsions and paroxysmal choreoathetosis, familial (C535522) ........Myokymia with neonatal epilepsy (C536099) ........SEIZURES, BENIGN FAMILIAL INFANTILE, 2 (OMIM:605751) ........SEIZURES, BENIGN FAMILIAL NEONATAL, 1 (OMIM:121200) ........SEIZURES, BENIGN FAMILIAL NEONATAL, 2 (OMIM:121201) Sister Nodes: ..Amniotic Band Syndrome (D000652) 3 ..Anemia, Neonatal (D000751) 2 ..Asphyxia Neonatorum (D001238) 1 ..Birth Injuries (D001720) 1 ..Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal (C563463) ..Congenital Hyperinsulinism (D044903) 2 ..Cutis Laxa-Marfanoid Syndrome (C563639) ..Cystic Fibrosis (D003550) 4 ..Developmental Delay, Epilepsy, and Neonatal Diabetes (C565253) ..Diabetes Mellitus, Transient Neonatal, 1 (C563322) ..Diabetes Mellitus, Transient Neonatal, 2 (C563672) ..Epilepsy, Benign Neonatal (D020936) 13 ..Erythroblastosis, Fetal (D004899) 7 ..Hernia, Umbilical (D006554) 6 ..Hydrophthalmos (D006871) ..Hyperbilirubinemia, Neonatal (D051556) 4 ..Hypercalcemia, Idiopathic, of Infancy (C562581) ..Hyperglycinemia, Transient Neonatal (C562672) ..Hyperostosis, Cortical, Congenital (D006958) 6 ..Hyperparathyroidism, Neonatal Severe Primary (C563375) ..Hypoglycemia, Neonatal, Simulating Foetopathia Diabetica (C565484) ..Ichthyosis (D007057) 66 ..Infant, Premature, Diseases (D007235) 14 ..Meconium Aspiration Syndrome (D008471) ..Mobius Syndrome (D020331) 4 ..Neonatal Abstinence Syndrome (D009357) ..Nystagmus, Congenital (D020417) 17 ..Ophthalmia Neonatorum (D009878) ..Persistent Fetal Circulation Syndrome (D010547) 1 ..Rothmund-Thomson Syndrome (D011038) 5 ..Sclerema Neonatorum (D012593) ..Severe Combined Immunodeficiency (D016511) 22 ..Syphilis, Congenital (D013590) ..Thanatophoric Dysplasia (D013796) 8 ..Thrombocytopenia, Neonatal Alloimmune (D054098) ..Toxoplasmosis, Congenital (D014125) ..Vitamin K Deficiency Bleeding (D006475) ..Wolman Disease (D015223) 2 Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 3854
Name: Epilepsy, Benign Neonatal
Definition: 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)
Alternative IDs: OMIM:601764
ParentIDs: MESH:D004827|MESH:D007232
TreeNumbers: C10.228.140.490.370 |C16.614.258
Synonyms: Benign Familial Infantile Convulsions |Benign Familial Infantile Convulsions Syndrome |Benign Familial Neonatal Convulsions |Benign Familial Neonatal Epilepsy |Benign Familial Neonatal Infantile Seizures |Benign Familial Neonatal-Infantile Seizures |Benign Inf
Slim Mappings: Infant-newborn disease|Nervous system disease
Reference:
MedGen: D020936
MeSH: D020936
OMIM: 601764 ; Genes: Phenotypes Disease Causing ClinVar Variants