Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13
CUI: C0302142
Disease: Deformity
Deformity 		0.040 Biomarker BEFREE The results from the in vivo experiments showed that BDE-209 resulted in damage to the testis structure, led to cell apoptosis in testis and decreased sperm number and motility, while sperm malformation rates were significantly increased. 31520908

2019
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13
CUI: C0302142
Disease: Deformity
Deformity 		0.040 Biomarker BEFREE The affected subjects in this family had no other clinical malformation beyond SPD. 31306809

2019
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13
CUI: C0302142
Disease: Deformity
Deformity 		0.040 GeneticVariation BEFREE Synpolydactyly (SPD) is an autosomal dominant malformation of the distal limbs caused by mutations in the homeobox gene HOXD13 located on chromosome 2q31. 16497573

2006
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13
CUI: C0302142
Disease: Deformity
Deformity 		0.040 Biomarker BEFREE Synpolydactyly (SPD) is a rare malformation of the distal limbs known to be caused by mutations in HOXD13. 10951517

2000