HOXD13, homeobox D13, 3239

N. diseases: 259; N. variants: 19
Disease: VATER Association ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0220708
Disease: VATER Association
VATER Association 		0.500 Biomarker disease CTD_human Identification of a HOXD13 mutation in a VACTERL patient. 19006232 2008
CUI: C0220708
Disease: VATER Association
VATER Association 		0.500 GeneticVariation disease ORPHANET Identification of a HOXD13 mutation in a VACTERL patient. 19006232 2008