Disease: Benign neonatal epilepsy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0270851
Disease: Benign neonatal epilepsy
Benign neonatal epilepsy 		0.010 Biomarker disease BEFREE Mutation analysis made KCNQ5 unlikely as a candidate gene for benign neonatal convulsions in patients with a positive family history for neonatal or early infantile seizures, but without mutations in the KCNQ2 or KCNQ3 genes. 10884071 2000