Details of Disease | DrugMAP

General Information of Disease (ID: DIS6LZ05)

Disease Name	Seizures, benign familial infantile, 2
Synonyms	convulsions, benign familial infantile, 2; BFIS2; seizures, benign familial infantile, type 2; seizures, benign familial infantile, 2
Disease Hierarchy	DISFYXOW: Benign familial infantile epilepsy DIS6LZ05: Seizures, benign familial infantile, 2
Disease Identifiers	MONDO ID MONDO_0011593 MESH ID C565296 UMLS CUI C1853995 OMIM ID 605751 MedGen ID 381313

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
PRRT2	OTCJUBDO	Strong	Autosomal dominant	[1]
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References

1	The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.