WDR35, WD repeat domain 35, 57539

N. diseases: 188; N. variants: 30
Disease: Craniosynostosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		0.410 GeneticVariation disease BEFREE We review 39 patients including two new patients, one with compound heterozygous novel mutations in WDR35 and a previously unreported multisutural craniosynostosis that may be a part of Sensenbrenner syndrome. 24123776 2013
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		0.410 Biomarker disease CTD_human Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome. 20817137 2010
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		0.410 Biomarker disease HPO