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: C0152240
Disease: Uterus bilocularis
Uterus bilocularis 		0.200 Biomarker disease MGD Hoxa-13 gene mutation results in abnormal seminal vesicle and prostate development. 10210434 1999
CUI: C0152240
Disease: Uterus bilocularis
Uterus bilocularis 		0.200 Biomarker disease MGD Infertility in adult hypodactyly mice is associated with hypoplasia of distal reproductive structures. 10569982 1999
CUI: C0478044
Disease: Other doubling of uterus
Other doubling of uterus 		0.200 Biomarker disease MGD Infertility in adult hypodactyly mice is associated with hypoplasia of distal reproductive structures. 10569982 1999
CUI: C0478044
Disease: Other doubling of uterus
Other doubling of uterus 		0.200 Biomarker disease MGD Hoxa-13 gene mutation results in abnormal seminal vesicle and prostate development. 10210434 1999
CUI: C0152240
Disease: Uterus bilocularis
Uterus bilocularis 		0.200 Biomarker disease MGD Hypodactyly, a semidominant lethal mutation in mice. 5519671 1971
CUI: C0478044
Disease: Other doubling of uterus
Other doubling of uterus 		0.200 Biomarker disease MGD Hypodactyly, a semidominant lethal mutation in mice. 5519671 1971
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
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion 		0.100 Biomarker phenotype HPO
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.100 Biomarker group HPO
CUI: C0034186
Disease: Pyelonephritis
Pyelonephritis 		0.100 Biomarker disease HPO
CUI: C0038379
Disease: Strabismus
Strabismus 		0.100 Biomarker disease HPO
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux 		0.100 Biomarker disease HPO
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		0.100 Biomarker disease HPO
CUI: C0221182
Disease: Chordee
Chordee 		0.100 Biomarker disease HPO
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection 		0.100 Biomarker disease HPO
CUI: C0266387
Disease: Bicornuate uterus
Bicornuate uterus 		0.100 Biomarker disease HPO
CUI: C0266393
Disease: Congenital duplication of uterus
Congenital duplication of uterus 		0.100 Biomarker disease HPO
CUI: C0341787
Disease: Bifid scrotum
Bifid scrotum 		0.100 Biomarker disease HPO
CUI: C0426848
Disease: Sacral dimple
Sacral dimple 		0.100 Biomarker phenotype HPO
CUI: C0431890
Disease: Hypoplasia of thumb
Hypoplasia of thumb 		0.100 Biomarker disease HPO
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers 		0.100 Biomarker disease HPO
CUI: C0432333
Disease: Abnormal dermatoglyphic pattern
Abnormal dermatoglyphic pattern 		0.100 Biomarker disease HPO
CUI: C0452168
Disease: Hypospadias, balanic
Hypospadias, balanic 		0.100 Biomarker disease HPO
CUI: C0521619
Disease: Obstruction of pelviureteric junction
Obstruction of pelviureteric junction 		0.100 Biomarker phenotype HPO