Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9681
Gene Symbol: DEPDC5
DEPDC5
CUI: C0036572
Disease: Seizures
Seizures 		0.150 CausalMutation CLINVAR Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5. 26000329

2015
Entrez Id: 9681
Gene Symbol: DEPDC5
DEPDC5
CUI: C0036572
Disease: Seizures
Seizures 		0.150 CausalMutation CLINVAR Epileptic spasms are a feature of DEPDC5 mTORopathy. 27066554

2015
Entrez Id: 9681
Gene Symbol: DEPDC5
DEPDC5
CUI: C0036572
Disease: Seizures
Seizures 		0.150 CausalMutation CLINVAR Novel DEPDC5 mutations causing familial focal epilepsy with variable foci identified. 23869883

2013
Entrez Id: 9681
Gene Symbol: DEPDC5
DEPDC5
CUI: C0036572
Disease: Seizures
Seizures 		0.150 CausalMutation CLINVAR Mutations in DEPDC5 cause familial focal epilepsy with variable foci. 23542697

2013