Seizures, benign familial infantile, 3
Also known as BFNIS, SCN2A benign familial infantile epilepsy, benign familial infantile epilepsy caused by mutation in SCN2A, benign familial neonatal-infantile seizures+8 more
BFNIS, SCN2A benign familial infantile epilepsy, benign familial infantile epilepsy caused by mutation in SCN2A, benign familial neonatal-infantile seizures, benign neonatal-infantile epilepsy, seizures, benign familial infantile, type 3, BFIS3, benign familial infantile convulsions, convulsions benign familial neonatal, convulsions, benign familial infantile, 3, epilepsy, benign neonatal-infantile, seizures, benign familial neonatal-infantile.
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An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
BFNIS, SCN2A benign familial infantile epilepsy, benign familial infantile epilepsy caused by mutation in SCN2A, benign familial neonatal-infantile seizures, benign neonatal-infantile epilepsy, seizures, benign familial infantile, type 3, BFIS3, benign familial infantile convulsions, convulsions benign familial neonatal, convulsions, benign familial infantile, 3, epilepsy, benign neonatal-infantile, seizures, benign familial neonatal-infantile
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.