Gene: HOXD13 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 GeneticVariation phenotype UNIPROT Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families. 24789103 2014
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 Biomarker phenotype CTD_human Human HOX gene disorders. 24239177 2014
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 Biomarker phenotype GENOMICS_ENGLAND Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome. 17236141 2007
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 GeneticVariation phenotype UNIPROT Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E. 12649808 2003
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 Biomarker phenotype GENOMICS_ENGLAND Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E. 12649808 2003
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 Biomarker phenotype GENOMICS_ENGLAND
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 CausalMutation phenotype CLINVAR
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 Biomarker phenotype HPO