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Disease Browser
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Epilepsy (D004827)
Parent Node:
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Infant, Newborn, Diseases (D007232)
..Starting node
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Epilepsy, Benign Neonatal (D020936)

       Child Nodes:
........expandConvulsions benign familial neonatal dominant form (C535466)
........expandConvulsions, Benign Familial Infantile, 4 (C567231)
........expandConvulsions, Benign Familial Neonatal, 1, And/Or Myokymia (C567744)
........expandConvulsions, Benign Familial Neonatal, 1, Atypical Severe (C567746)
........expandEpilepsy, Benign Neonatal, 1 (C565164)
........expandEpilepsy, Benign Neonatal, 1, Atypical Severe (C567745)
........expandEpilepsy, Benign Neonatal, 3 (C564274)
........expandEpilepsy, Benign Neonatal, Autosomal Recessive (C564823)
........expandInfantile convulsions and paroxysmal choreoathetosis, familial (C535522)
........expandMyokymia with neonatal epilepsy (C536099)
........expandSEIZURES, BENIGN FAMILIAL INFANTILE, 2 (OMIM:605751)
........expandSEIZURES, BENIGN FAMILIAL NEONATAL, 1 (OMIM:121200)
........expandSEIZURES, BENIGN FAMILIAL NEONATAL, 2 (OMIM:121201)



 Sister Nodes: 
..expandAmniotic Band Syndrome (D000652) Child3
..expandAnemia, Neonatal (D000751) Child2
..expandAsphyxia Neonatorum (D001238) Child1
..expandBirth Injuries (D001720) Child1
..expandCarnitine Palmitoyltransferase II Deficiency, Lethal Neonatal (C563463)
..expandCongenital Hyperinsulinism (D044903) Child2
..expandCutis Laxa-Marfanoid Syndrome (C563639)
..expandCystic Fibrosis (D003550) Child4
..expandDevelopmental Delay, Epilepsy, and Neonatal Diabetes (C565253)
..expandDiabetes Mellitus, Transient Neonatal, 1 (C563322)
..expandDiabetes Mellitus, Transient Neonatal, 2 (C563672)
..expandEpilepsy, Benign Neonatal (D020936) Child13
..expandErythroblastosis, Fetal (D004899) Child7
..expandHernia, Umbilical (D006554) Child6
..expandHydrophthalmos (D006871)
..expandHyperbilirubinemia, Neonatal (D051556) Child4
..expandHypercalcemia, Idiopathic, of Infancy (C562581)
..expandHyperglycinemia, Transient Neonatal (C562672)
..expandHyperostosis, Cortical, Congenital (D006958) Child6
..expandHyperparathyroidism, Neonatal Severe Primary (C563375)
..expandHypoglycemia, Neonatal, Simulating Foetopathia Diabetica (C565484)
..expandIchthyosis (D007057) Child66
..expandInfant, Premature, Diseases (D007235) Child14
..expandMeconium Aspiration Syndrome (D008471)
..expandMobius Syndrome (D020331) Child4
..expandNeonatal Abstinence Syndrome (D009357)
..expandNystagmus, Congenital (D020417) Child17
..expandOphthalmia Neonatorum (D009878)
..expandPersistent Fetal Circulation Syndrome (D010547) Child1
..expandRothmund-Thomson Syndrome (D011038) Child5
..expandSclerema Neonatorum (D012593)
..expandSevere Combined Immunodeficiency (D016511) Child22
..expandSyphilis, Congenital (D013590)
..expandThanatophoric Dysplasia (D013796) Child8
..expandThrombocytopenia, Neonatal Alloimmune (D054098)
..expandToxoplasmosis, Congenital (D014125)
..expandVitamin K Deficiency Bleeding (D006475)
..expandWolman Disease (D015223) Child2
   

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
1 HP:0000006Autosomal dominant inheritance
2 HP:0007334Bilateral tonic-clonic seizure with focal onset
3 HP:0000961Cyanosis
4 HP:0011146Dialeptic seizure
5 HP:0001425Heterogeneous
6 HP:0002372Normal interictal EEG
7 HP:0040168obsolete Focal seizures, afebril
Disease Causing ClinVar Variants