Disease: Flatfoot ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0016202
Disease: Flatfoot
Flatfoot 		0.110 GeneticVariation phenotype BEFREE Here we report a 62 kb de novo deletion encompassing exon 6 of AUTS2 detected by chromosomal microarray analysis (CMA) in a 4.5 year-old female patient with severe speech and language disorder, history of tonic-clonic movements, and pes planus with eversion of the feet. 24459036 2014
CUI: C0016202
Disease: Flatfoot
Flatfoot 		0.110 GeneticVariation phenotype CLINVAR