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: C2212006
Disease: Small cell carcinoma of ovary
Small cell carcinoma of ovary 		2 0 1 0.14 0 0
CUI: C3150215
Disease: CHROMOSOME 6q24-q25 DELETION SYNDROME
CHROMOSOME 6q24-q25 DELETION SYNDROME 		2 0 1 0.14 0 0
CUI: C4020917
Disease: Absent fifth fingernail
Absent fifth fingernail 		2 0 1 0.14 0 0
CUI: C1832348
Disease: Slow-growing hair
Slow-growing hair 		35 0 5 0.14 0 0
CUI: C0265372
Disease: Fetal hydantoin syndrome
Fetal hydantoin syndrome 		11 0 2 0.13 0 0
CUI: C0431368
Disease: Partial agenesis of corpus callosum
Partial agenesis of corpus callosum 		38 0 5 0.13 0 0
CUI: C0039981
Disease: Thoracic Neoplasms
Thoracic Neoplasms 		3 0 1 0.12 0 0
CUI: C0266324
Disease: Congenital dilatation of ureter
Congenital dilatation of ureter 		3 1 1 0.12 1 1.6E-02
CUI: C0474809
Disease: Endometrioid tumor
Endometrioid tumor 		3 0 1 0.12 0 0
CUI: C2985524
Disease: Rhabdoid tumor predisposition syndrome
Rhabdoid tumor predisposition syndrome 		3 0 1 0.12 0 0
CUI: C4021892
Disease: Absent fifth toenail
Absent fifth toenail 		3 0 1 0.12 0 0
CUI: C4289955
Disease: Atypical Endometriosis
Atypical Endometriosis 		3 0 1 0.12 0 0
CUI: C4021735
Disease: Abnormality of the hip bone
Abnormality of the hip bone 		40 0 5 0.12 0 0
CUI: C0238207
Disease: Ectopic kidney
Ectopic kidney 		41 0 5 0.12 0 0
CUI: C4021792
Disease: Abnormality of the clavicle
Abnormality of the clavicle 		42 0 5 0.12 0 0
CUI: C0265881
Disease: Congenital hypoplasia of aortic arch
Congenital hypoplasia of aortic arch 		4 0 1 0.11 0 0
CUI: C1516865
Disease: Endometrial Undifferentiated Carcinoma
Endometrial Undifferentiated Carcinoma 		4 0 1 0.11 0 0
CUI: C0265338
Disease: Coffin-Siris syndrome
Coffin-Siris syndrome 		56 6 6 0.11 1 1.5E-02
CUI: C0346167
Disease: Undifferentiated carcinoma of ovary
Undifferentiated carcinoma of ovary 		5 0 1 1.0E-01 0 0
CUI: C3551915
Disease: MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO
MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO 		5 0 1 1.0E-01 0 0
CUI: C4073145
Disease: Hyperkeratosis pilaris
Hyperkeratosis pilaris 		5 3 1 1.0E-01 1 1.6E-02
CUI: C1333989
Disease: Familial meningioma
Familial meningioma 		6 0 1 9.1E-02 0 0
CUI: C1836674
Disease: Short distal phalanx of the 5th finger
Short distal phalanx of the 5th finger 		6 0 1 9.1E-02 0 0
CUI: C3277940
Disease: Generalized hypertrichosis
Generalized hypertrichosis 		6 4 1 9.1E-02 1 1.6E-02
CUI: C0007118
Disease: Carcinoma, Basosquamous
Carcinoma, Basosquamous 		7 0 1 8.3E-02 0 0