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: C3839681
Disease: Seromucinous borderline tumor
Seromucinous borderline tumor 		1 0 1 1.0E-01 0 0
CUI: C4016770
Disease: CONOTRUNCAL ANOMALY FACE SYNDROME/VELOCARDIOFACIAL SYNDROME
CONOTRUNCAL ANOMALY FACE SYNDROME/VELOCARDIOFACIAL SYNDROME 		1 0 1 1.0E-01 0 0
CUI: C4024723
Disease: Decreased proportion circulating T-helper cells
Decreased proportion circulating T-helper cells 		1 0 1 1.0E-01 0 0
CUI: C4024990
Disease: Aplasia/Hypoplasia of the sternum
Aplasia/Hypoplasia of the sternum 		1 0 1 1.0E-01 0 0
CUI: C4302907
Disease: Agenesis of internal carotid artery
Agenesis of internal carotid artery 		1 0 1 1.0E-01 0 0
CUI: C4479229
Disease: HYPERPARATHYROIDISM 4
HYPERPARATHYROIDISM 4 		1 0 1 1.0E-01 0 0
CUI: C0152216
Disease: Esophoria
Esophoria 		2 0 1 9.1E-02 0 0
CUI: C0333155
Disease: Calcifying cyst
Calcifying cyst 		2 0 1 9.1E-02 0 0
CUI: C0342344
Disease: Hypoparathyroidism - X-linked
Hypoparathyroidism - X-linked 		2 0 1 9.1E-02 0 0
CUI: C0345065
Disease: Cervical aortic arch
Cervical aortic arch 		2 0 1 9.1E-02 0 0
CUI: C0559359
Disease: Subchondral hematoma
Subchondral hematoma 		2 0 1 9.1E-02 0 0
CUI: C0847415
Disease: facet joint degeneration
facet joint degeneration 		2 0 1 9.1E-02 0 0
CUI: C1266049
Disease: Hyalinizing trabecular adenoma
Hyalinizing trabecular adenoma 		2 0 1 9.1E-02 0 0
CUI: C1869118
Disease: HYPOTHYROIDISM, CONGENITAL, DUE TO THYROID DYSGENESIS
HYPOTHYROIDISM, CONGENITAL, DUE TO THYROID DYSGENESIS 		2 0 1 9.1E-02 0 0
CUI: C2212006
Disease: Small cell carcinoma of ovary
Small cell carcinoma of ovary 		2 0 1 9.1E-02 0 0
CUI: C3151189
Disease: C9 Deficiency
C9 Deficiency 		2 0 1 9.1E-02 0 0
CUI: C3898144
Disease: Neurovascular Disorder
Neurovascular Disorder 		2 0 1 9.1E-02 0 0
CUI: C4025175
Disease: Congenital alopecia totalis
Congenital alopecia totalis 		2 0 1 9.1E-02 0 0
CUI: C4025717
Disease: Abnormality of the small intestine
Abnormality of the small intestine 		2 0 1 9.1E-02 0 0
CUI: C4049490
Disease: Extragenital endometriosis
Extragenital endometriosis 		2 0 1 9.1E-02 0 0
CUI: C4733128
Disease: familial chordoma
familial chordoma 		2 0 1 9.1E-02 0 0
CUI: C4744527
Disease: Temporal Lobe Pleomorphic Xanthoastrocytoma
Temporal Lobe Pleomorphic Xanthoastrocytoma 		2 0 1 9.1E-02 0 0
CUI: C0155336
Disease: Esotropia with accommodative compensation
Esotropia with accommodative compensation 		3 0 1 8.3E-02 0 0
CUI: C0206369
Disease: Splenosis
Splenosis 		3 0 1 8.3E-02 0 0
CUI: C0265992
Disease: alopecia congenita
alopecia congenita 		3 0 1 8.3E-02 0 0