Gene: WDR45 ×
Source: INFERRED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11152
Gene Symbol: WDR45
WDR45 		0.140 GeneticVariation phenotype 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 		0.140 GeneticVariation phenotype 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 		0.140 GeneticVariation phenotype 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 		0.140 CausalMutation phenotype CLINVAR
Entrez Id: 11152
Gene Symbol: WDR45
WDR45 		0.140 Biomarker phenotype HPO