Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54982
Gene Symbol: CLN6
CLN6
CUI: C0036572
Disease: Seizures
Seizures 		0.110 GeneticVariation CLINVAR Novel mutations in the CLN6 gene causing a variant late infantile neuronal ceroid lipofuscinosis. 12673792

2003
Entrez Id: 54982
Gene Symbol: CLN6
CLN6
CUI: C0036572
Disease: Seizures
Seizures 		0.110 CausalMutation CLINVAR Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse. 11791207

2002
Entrez Id: 54982
Gene Symbol: CLN6
CLN6
CUI: C0036572
Disease: Seizures
Seizures 		0.110 Biomarker HPO