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: C1855675
Disease: Arima syndrome
Arima syndrome 		11 0 3 7.9E-02 0 0
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris 		52 0 6 7.9E-02 0 0
CUI: C2936476
Disease: Chronic Liver Failure
Chronic Liver Failure 		25 0 4 7.8E-02 0 0
CUI: C0151746
Disease: Abnormal renal function
Abnormal renal function 		12 6 3 7.7E-02 5 0.33
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		26 0 4 7.7E-02 0 0
CUI: C0265541
Disease: Cranioschisis
Cranioschisis 		12 0 3 7.7E-02 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder) 		27 0 4 7.5E-02 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		42 0 5 7.5E-02 0 0
CUI: C0521573
Disease: Coloboma of eyelid
Coloboma of eyelid 		28 0 4 7.4E-02 0 0
CUI: C0267818
Disease: Bile duct proliferation
Bile duct proliferation 		30 0 4 7.1E-02 0 0
CUI: C0311245
Disease: Congenital cystic kidney disease
Congenital cystic kidney disease 		31 0 4 7.0E-02 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea 		31 0 4 7.0E-02 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 8 6.8E-02 0 0
CUI: C0235259
Disease: Subcapsular cataract
Subcapsular cataract 		17 0 3 6.8E-02 0 0
CUI: C4020869
Disease: Abnormality of abdomen morphology
Abnormality of abdomen morphology 		17 0 3 6.8E-02 0 0
CUI: C0221365
Disease: Double ureter
Double ureter 		34 0 4 6.7E-02 0 0
CUI: C1835698
Disease: Keratitis, hereditary
Keratitis, hereditary 		2 2 2 6.7E-02 2 0.14
CUI: C1837819
Disease: Cerebrofrontofacial Syndrome
Cerebrofrontofacial Syndrome 		2 0 2 6.7E-02 0 0
CUI: C3805604
Disease: FOVEAL HYPOPLASIA 1
FOVEAL HYPOPLASIA 1 		2 4 2 6.7E-02 2 0.12
CUI: C4025234
Disease: Duplication of internal organs
Duplication of internal organs 		2 0 2 6.7E-02 0 0
CUI: C4072884
Disease: Ciliary body coloboma
Ciliary body coloboma 		2 0 2 6.7E-02 0 0
CUI: C4021813
Disease: Oral cleft
Oral cleft 		85 0 7 6.5E-02 0 0
CUI: C0040412
Disease: Fissured tongue
Fissured tongue 		36 0 4 6.5E-02 0 0
CUI: C0344543
Disease: Aniridia type 2
Aniridia type 2 		3 0 2 6.5E-02 0 0
CUI: C0549307
Disease: Morning glory syndrome
Morning glory syndrome 		3 0 2 6.5E-02 0 0