Details of Disease | DrugMAP

General Information of Disease (ID: DISQVTP9)

Disease Name	Obsolete benign familial neonatal-infantile seizures
Disease Hierarchy	DIS01GPL: Grass pollen hypersensitivity DISQVTP9: Obsolete benign familial neonatal-infantile seizures

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 2 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
KCNQ2	TTPXI3S	Supportive	Autosomal dominant	[1]
SCN2A	TTLJTUF	Supportive	Autosomal dominant	[2]
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This Disease Is Related to 2 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
KCNQ2	OT3CXQJT	Supportive	Autosomal dominant	[1]
SCN2A	OTUSYE4Z	Supportive	Autosomal dominant	[2]
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References

1	Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance. Epilepsia. 2013 Mar;54(3):425-36. doi: 10.1111/epi.12089. Epub 2013 Jan 29.
2	Sodium-channel defects in benign familial neonatal-infantile seizures. Lancet. 2002 Sep 14;360(9336):851-2. doi: 10.1016/S0140-6736(02)09968-3.