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Disease

Seizures, benign familial infantile, 5

Also known as BFIS5, SCN8A benign familial infantile epilepsy, benign familial infantile epilepsy caused by mutation in SCN8A, seizures, benign familial infantile, 5; BFIS5+2 more

BFIS5, SCN8A benign familial infantile epilepsy, benign familial infantile epilepsy caused by mutation in SCN8A, seizures, benign familial infantile, 5; BFIS5, seizures, benign familial infantile, type 5, convulsions, benign familial infantile, 5.

1
Associated genes
1
Related proteins

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Associated genes

1 match

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

SCN8A0.77

Disease biology

1 match

Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.

Sodium channel protein type 8 subunit alphavia SCN8A0.77

Reference

Authoritative identity, definition & identifiers.

Synonyms

BFIS5, SCN8A benign familial infantile epilepsy, benign familial infantile epilepsy caused by mutation in SCN8A, seizures, benign familial infantile, 5; BFIS5, seizures, benign familial infantile, type 5, convulsions, benign familial infantile, 5

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.