Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23732
Gene Symbol: FRRS1L
FRRS1L
CUI: C0036572
Disease: Seizures
Seizures
0.100 CausalMutation CLINVAR Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy. 27236917

2016

Entrez Id: 23732
Gene Symbol: FRRS1L
FRRS1L
CUI: C0036572
Disease: Seizures
Seizures
0.100 Biomarker HPO