General Information of Disease (ID: DISV7PWN)

Disease Name Obsolete benign familial mesial temporal lobe epilepsy
Synonyms benign FMTLE
Definition
OBSOLETE. Benign familial mesial temporal lobe epilepsy is a rare epilepsy characterized by seizures with viscerosensory or experential auras, onset in adolescence or early adulthood and good prognosis. It is defined as at least 24 months of seizure freedom with or without antiepileptic medication.
Disease Hierarchy
DIS01GPL: Grass pollen hypersensitivity
DISV7PWN: Obsolete benign familial mesial temporal lobe epilepsy

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
CPA6 OT43RD23 Supportive Autosomal dominant [1]
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References

1 Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy. Hum Mutat. 2012 Jan;33(1):124-35. doi: 10.1002/humu.21613. Epub 2011 Oct 31.