HOXA13, homeobox A13, 3209

N. diseases: 126; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0221357
Disease: Brachydactyly
Brachydactyly
0.110 GeneticVariation disease BEFREE Mutations in HOXA13 and HOXD13 are associated with disorders of limb formation such as hand-foot-genital syndrome (HFGS), synpolydactyly (SPD), and brachydactyly. 15643670 2005
CUI: C0221357
Disease: Brachydactyly
Brachydactyly
0.110 Biomarker disease HPO