Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11152
Gene Symbol: WDR45
WDR45
CUI: C0036572
Disease: Seizures
Seizures 		0.140 GeneticVariation CLINVAR β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation. 23687123

2013
Entrez Id: 11152
Gene Symbol: WDR45
WDR45
CUI: C0036572
Disease: Seizures
Seizures 		0.140 GeneticVariation CLINVAR De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood. 23435086

2013
Entrez Id: 11152
Gene Symbol: WDR45
WDR45
CUI: C0036572
Disease: Seizures
Seizures 		0.140 GeneticVariation CLINVAR Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. 23176820

2012
Entrez Id: 11152
Gene Symbol: WDR45
WDR45
CUI: C0036572
Disease: Seizures
Seizures 		0.140 CausalMutation CLINVAR

Entrez Id: 11152
Gene Symbol: WDR45
WDR45
CUI: C0036572
Disease: Seizures
Seizures 		0.140 Biomarker HPO