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: C1834931
Disease: Cystic renal dysplasia
Cystic renal dysplasia 		12 0 6 6.3E-02 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI 		35 0 7 6.0E-02 0 0
CUI: C0032617
Disease: Polyuria
Polyuria 		73 0 9 5.9E-02 0 0
CUI: C3540764
Disease: Coloboma of the Retina
Coloboma of the Retina 		58 0 8 5.8E-02 0 0
CUI: C1854418
Disease: Biparietal narrowing
Biparietal narrowing 		60 0 8 5.7E-02 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		61 0 8 5.6E-02 0 0
CUI: C0267834
Disease: Liver cyst
Liver cyst 		26 0 6 5.5E-02 0 0
CUI: C4551568
Disease: Joubert syndrome 1
Joubert syndrome 1 		26 0 6 5.5E-02 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 6 5.4E-02 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 6 5.4E-02 0 0
CUI: C0020541
Disease: Portal Hypertension
Portal Hypertension 		167 0 13 5.3E-02 0 0
CUI: C0267818
Disease: Bile duct proliferation
Bile duct proliferation 		30 0 6 5.3E-02 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 6 5.3E-02 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 6 5.3E-02 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 6 5.3E-02 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea 		31 0 6 5.3E-02 0 0
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		93 0 9 5.2E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 15 5.2E-02 0 0
CUI: C3536714
Disease: Renal dysplasia
Renal dysplasia 		95 0 9 5.1E-02 0 0
CUI: C1865872
Disease: NEPHRONOPHTHISIS 2
NEPHRONOPHTHISIS 2 		14 0 5 5.1E-02 0 0
CUI: C0010709
Disease: Cyst
Cyst 		221 0 15 5.1E-02 0 0
CUI: C0240896
Disease: Fundus coloboma
Fundus coloboma 		57 0 7 5.0E-02 0 0
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia 		100 0 9 5.0E-02 0 0
CUI: C0158683
Disease: Polycystic liver disease
Polycystic liver disease 		38 0 6 5.0E-02 0 0
CUI: C1855681
Disease: Nephronophthisis, familial juvenile
Nephronophthisis, familial juvenile 		17 0 5 5.0E-02 0 0