Ontology Browser

Term:
Benign Familial Infantile Seizures, 5 (DOID:9003651)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
West syndrome +     
Autosomal Recessive Infantile Epilepsy  
Benign Familial Infantile Seizures, 2  
Benign Familial Infantile Seizures, 3  
Benign Familial Infantile Seizures, 4 
Benign Familial Infantile Seizures, 5  
An autosomal dominant neurologic disorder characterized by onset of afebrile seizures during infancy. (OMIM)
Benign Familial Neonatal Convulsions 1, Atypical Severe 
Benign Familial Neonatal Seizures, 1  
Benign Familial Neonatal Seizures, 2  
Benign Neonatal Epilepsy, 1  
Benign Neonatal Epilepsy, 1, Atypical Severe 
Benign Neonatal Epilepsy, Autosomal Recessive 
Epilepsy, Benign Neonatal, 1, and/or Myokymia 
Familial Infantile Convulsions and Paroxysmal Choreoathetosis  
Infantile or Early Childhood Epileptic Encephalopathy +   
Microcephaly, Corpus Callosum Dysgenesis and Cleft Lip-Palate 
Myokymia with Neonatal Epilepsy 
Norrie disease  
PEHO Syndrome  

Synonyms
Exact Synonyms: BFIC5 ;   BFIS5 ;   CONVULSIONS, BENIGN FAMILIAL INFANTILE, 5
Primary IDs: OMIM:617080
Alternate IDs: RDO:9001259

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.