HOXD10, homeobox D10, 3236

N. diseases: 83; N. variants: 3
Disease: Congenital vertical talus, bilateral ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1860446
Disease: Congenital vertical talus, bilateral
Congenital vertical talus, bilateral 		0.300 GermlineCausalMutation phenotype ORPHANET HOXD10 M319K mutation in a family with isolated congenital vertical talus. 16450407 2006
CUI: C1860446
Disease: Congenital vertical talus, bilateral
Congenital vertical talus, bilateral 		0.300 GermlineCausalMutation phenotype ORPHANET A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease. 15146389 2004