Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		0.300 Biomarker CTD_human Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome. 20817137

2010