WDR35, WD repeat domain 35, 57539

N. diseases: 188; N. variants: 30
Disease: Craniosynostosis, Type 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551902
Disease: Craniosynostosis, Type 1
Craniosynostosis, Type 1 		0.300 Biomarker disease CTD_human Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome. 20817137 2010