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: C0003910
Disease: Articulation Disorders
Articulation Disorders 		1 0 1 0.20 0 0
CUI: C0231912
Disease: Nocturnal cough
Nocturnal cough 		1 0 1 0.20 0 0
CUI: C0265756
Disease: Congenital atresia of larynx
Congenital atresia of larynx 		1 0 1 0.20 0 0
CUI: C0266320
Disease: Impervious ureter
Impervious ureter 		1 0 1 0.20 0 0
CUI: C1857455
Disease: Extension of hair growth on temples to lateral eyebrow
Extension of hair growth on temples to lateral eyebrow 		1 0 1 0.20 0 0
CUI: C1960046
Disease: Mild persistent asthma
Mild persistent asthma 		1 0 1 0.20 0 0
CUI: C1971810
Disease: Congenital cardiovascular disorder
Congenital cardiovascular disorder 		1 0 1 0.20 0 0
CUI: C2675369
Disease: Chromosome 22q11.2 Microduplication Syndrome
Chromosome 22q11.2 Microduplication Syndrome 		1 0 1 0.20 0 0
CUI: C3531771
Disease: Dextrotransposition of the great arteries
Dextrotransposition of the great arteries 		1 0 1 0.20 0 0
CUI: C4016770
Disease: CONOTRUNCAL ANOMALY FACE SYNDROME/VELOCARDIOFACIAL SYNDROME
CONOTRUNCAL ANOMALY FACE SYNDROME/VELOCARDIOFACIAL SYNDROME 		1 0 1 0.20 0 0
CUI: C4024990
Disease: Aplasia/Hypoplasia of the sternum
Aplasia/Hypoplasia of the sternum 		1 0 1 0.20 0 0
CUI: C0152216
Disease: Esophoria
Esophoria 		2 0 1 0.17 0 0
CUI: C0345065
Disease: Cervical aortic arch
Cervical aortic arch 		2 0 1 0.17 0 0
CUI: C0936243
Disease: HIV-1-Associated Cognitive Motor Complex
HIV-1-Associated Cognitive Motor Complex 		2 0 1 0.17 0 0
CUI: C2985307
Disease: Maternal Hypotension
Maternal Hypotension 		2 0 1 0.17 0 0
CUI: C3151189
Disease: C9 Deficiency
C9 Deficiency 		2 0 1 0.17 0 0
CUI: C4025717
Disease: Abnormality of the small intestine
Abnormality of the small intestine 		2 0 1 0.17 0 0
CUI: C4310653
Disease: LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME
LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME 		2 0 1 0.17 0 0
CUI: C4733128
Disease: familial chordoma
familial chordoma 		2 0 1 0.17 0 0
CUI: C4744527
Disease: Temporal Lobe Pleomorphic Xanthoastrocytoma
Temporal Lobe Pleomorphic Xanthoastrocytoma 		2 0 1 0.17 0 0
CUI: C0392485
Disease: Congenital diverticulum of pharynx
Congenital diverticulum of pharynx 		10 0 2 0.15 0 0
CUI: C0155336
Disease: Esotropia with accommodative compensation
Esotropia with accommodative compensation 		3 0 1 0.14 0 0
CUI: C0849925
Disease: Ventricular failure
Ventricular failure 		3 0 1 0.14 0 0
CUI: C1266175
Disease: Parachordoma
Parachordoma 		3 0 1 0.14 0 0
CUI: C1322281
Disease: Seasonal rhinitis
Seasonal rhinitis 		3 0 1 0.14 0 0