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: C1858033
Disease: Asymmetry of the thorax
Asymmetry of the thorax 		12 0 3 8.3E-02 0 0
CUI: C1853737
Disease: Prominent occiput
Prominent occiput 		53 0 6 8.1E-02 0 0
CUI: C1320468
Disease: Nephrogenic rest
Nephrogenic rest 		15 0 3 7.7E-02 0 0
CUI: C0311245
Disease: Congenital cystic kidney disease
Congenital cystic kidney disease 		31 0 4 7.4E-02 0 0
CUI: C1839277
Disease: Submucous cleft lip
Submucous cleft lip 		2 0 2 7.4E-02 0 0
CUI: C1839279
Disease: Six lumbar vertebrae
Six lumbar vertebrae 		2 0 2 7.4E-02 0 0
CUI: C1839285
Disease: Two carpal ossification centers present at birth
Two carpal ossification centers present at birth 		2 0 2 7.4E-02 0 0
CUI: C1856361
Disease: Doll-like facies
Doll-like facies 		2 0 2 7.4E-02 0 0
CUI: C2930471
Disease: Bilateral Wilms Tumor
Bilateral Wilms Tumor 		31 0 4 7.4E-02 0 0
CUI: C2931228
Disease: VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS
VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS 		2 0 2 7.4E-02 0 0
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome 		107 0 9 7.2E-02 0 0
CUI: C1839269
Disease: Duplication of renal pelvis
Duplication of renal pelvis 		3 0 2 7.1E-02 0 0
CUI: C1849765
Disease: Absence of renal corticomedullary differentiation
Absence of renal corticomedullary differentiation 		3 0 2 7.1E-02 0 0
CUI: C2673883
Disease: RENAL-HEPATIC-PANCREATIC DYSPLASIA
RENAL-HEPATIC-PANCREATIC DYSPLASIA 		3 0 2 7.1E-02 0 0
CUI: C3887743
Disease: WILMS TUMOR 2
WILMS TUMOR 2 		3 0 2 7.1E-02 0 0
CUI: C4543692
Disease: Anxiety in pregnancy
Anxiety in pregnancy 		3 0 2 7.1E-02 0 0
CUI: C0339477
Disease: Lipidemia retinalis
Lipidemia retinalis 		4 0 2 6.9E-02 0 0
CUI: C1839276
Disease: Broad secondary alveolar ridge
Broad secondary alveolar ridge 		4 0 2 6.9E-02 0 0
CUI: C1866689
Disease: Short sacroiliac notch
Short sacroiliac notch 		4 0 2 6.9E-02 0 0
CUI: C4551509
Disease: Jervell And Lange-Nielsen Syndrome 1
Jervell And Lange-Nielsen Syndrome 1 		4 0 2 6.9E-02 0 0
CUI: C0024421
Disease: Macroglossia
Macroglossia 		115 0 9 6.8E-02 0 0
CUI: C0266345
Disease: Congenital urethral valve
Congenital urethral valve 		5 0 2 6.7E-02 0 0
CUI: C1848599
Disease: VACTERL Association With Hydrocephalus
VACTERL Association With Hydrocephalus 		5 0 2 6.7E-02 0 0
CUI: C1865877
Disease: Renal cortical microcysts
Renal cortical microcysts 		5 0 2 6.7E-02 0 0
CUI: C1868139
Disease: Medullary cystic kidney disease 1
Medullary cystic kidney disease 1 		5 0 2 6.7E-02 0 0