Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0332890
Disease: Congenital hemihypertrophy
Congenital hemihypertrophy 		23 0 9 0.13 0 0
CUI: C1840382
Disease: Abnormality of the ureter
Abnormality of the ureter 		19 0 8 0.12 0 0
CUI: C1857949
Disease: Prominent metopic ridge
Prominent metopic ridge 		39 0 10 0.12 0 0
CUI: C0265677
Disease: Congenital hemivertebra
Congenital hemivertebra 		49 0 11 0.12 0 0
CUI: C0432163
Disease: Defect of vertebral segmentation
Defect of vertebral segmentation 		40 0 10 0.12 0 0
CUI: C1851720
Disease: Adrenocortical cytomegaly
Adrenocortical cytomegaly 		6 0 6 0.11 0 0
CUI: C1851722
Disease: Overgrowth of external genitalia
Overgrowth of external genitalia 		6 0 6 0.11 0 0
CUI: C1851733
Disease: Pancreatic hyperplasia
Pancreatic hyperplasia 		6 0 6 0.11 0 0
CUI: C1853296
Disease: SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3
SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3 		6 0 6 0.11 0 0
CUI: C1837549
Disease: SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2
SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2 		7 0 6 0.11 0 0
CUI: C4021539
Disease: Posterior helix pit
Posterior helix pit 		9 0 6 0.11 0 0
CUI: C0426789
Disease: Short thorax
Short thorax 		51 0 10 0.11 0 0
CUI: C4025900
Disease: Abnormality of female internal genitalia
Abnormality of female internal genitalia 		31 0 8 0.11 0 0
CUI: C0265343
Disease: Jarcho-Levin syndrome
Jarcho-Levin syndrome 		12 0 6 0.10 0 0
CUI: C0235752
Disease: Port-Wine Stain
Port-Wine Stain 		46 0 9 1.0E-01 0 0
CUI: C1969144
Disease: Renal cortical cysts
Renal cortical cysts 		14 0 6 9.8E-02 0 0
CUI: C1839829
Disease: Short distal phalanx of finger
Short distal phalanx of finger 		85 0 12 9.5E-02 0 0
CUI: C4083048
Disease: SPONDYLOCOSTAL DYSOSTOSIS 5
SPONDYLOCOSTAL DYSOSTOSIS 5 		5 0 5 9.4E-02 0 0
CUI: C1849089
Disease: Broad forehead
Broad forehead 		133 0 16 9.4E-02 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		171 0 19 9.3E-02 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		137 0 16 9.2E-02 0 0
CUI: C1853246
Disease: Eversion of lower lip
Eversion of lower lip 		105 0 13 9.0E-02 0 0
CUI: C0221766
Disease: Diastasis recti
Diastasis recti 		22 0 6 8.7E-02 0 0
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele 		85 0 11 8.7E-02 0 0
CUI: C0432235
Disease: CRANIOECTODERMAL DYSPLASIA 1
CRANIOECTODERMAL DYSPLASIA 1 		10 0 5 8.6E-02 0 0