HOXD10, homeobox D10, 3236

N. diseases: 83; N. variants: 3
Disease: Flatfoot ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0016202
Disease: Flatfoot
Flatfoot 		0.300 Biomarker phenotype CTD_human Human HOX gene disorders. 24239177 2014
CUI: C0016202
Disease: Flatfoot
Flatfoot 		0.300 Biomarker phenotype CTD_human HOXD10 M319K mutation in a family with isolated congenital vertical talus. 16450407 2006
CUI: C0016202
Disease: Flatfoot
Flatfoot 		0.300 Biomarker phenotype CTD_human A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease. 15146389 2004