Gene: WDR26 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80232
Gene Symbol: WDR26
WDR26 		0.100 CausalMutation phenotype CLINVAR WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features. 28686853 2017