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: C0546982
Disease: Cystic fibrosis with meconium ileus
Cystic fibrosis with meconium ileus 		3 0 2 0.22 0 0
CUI: C4268639
Disease: Irritable bowel syndrome with constipation
Irritable bowel syndrome with constipation 		11 0 3 0.19 0 0
CUI: C0267509
Disease: Chronic idiopathic constipation
Chronic idiopathic constipation 		5 0 2 0.18 0 0
CUI: C4725093
Disease: Unresectable Melanoma
Unresectable Melanoma 		7 0 2 0.15 0 0
CUI: C0334263
Disease: Trichilemmoma
Trichilemmoma 		8 0 2 0.14 0 0
CUI: C0026718
Disease: Mucormycosis
Mucormycosis 		9 0 2 0.13 0 0
CUI: C0043541
Disease: Zygomycosis
Zygomycosis 		9 0 2 0.13 0 0
CUI: C0034066
Disease: Pulmonary embolism with pulmonary infarction
Pulmonary embolism with pulmonary infarction 		1 0 1 0.12 0 0
CUI: C0155820
Disease: Acute bronchitis and bronchiolitis
Acute bronchitis and bronchiolitis 		1 0 1 0.12 0 0
CUI: C0332882
Disease: congenital obstruction
congenital obstruction 		1 0 1 0.12 0 0
CUI: C0340037
Disease: Young Syndrome
Young Syndrome 		1 0 1 0.12 0 0
CUI: C0398349
Disease: Distal intestinal obstruction syndrome
Distal intestinal obstruction syndrome 		1 0 1 0.12 0 0
CUI: C0403819
Disease: Acquired obstructive azoospermia
Acquired obstructive azoospermia 		1 0 1 0.12 0 0
CUI: C0541798
Disease: Early Awakening
Early Awakening 		10 0 2 0.12 0 0
CUI: C0740266
Disease: Anal and rectal conditions
Anal and rectal conditions 		1 0 1 0.12 0 0
CUI: C0860006
Disease: Hypotonic dehydration
Hypotonic dehydration 		1 0 1 0.12 0 0
CUI: C0877664
Disease: Gastrointestinal cramps
Gastrointestinal cramps 		1 0 1 0.12 0 0
CUI: C0948783
Disease: Bronchopulmonary infection
Bronchopulmonary infection 		1 0 1 0.12 0 0
CUI: C1334425
Disease: Low Grade Malignant Neoplasm
Low Grade Malignant Neoplasm 		1 0 1 0.12 0 0
CUI: C1837893
Disease: SCHIZOPHRENIA 12
SCHIZOPHRENIA 12 		1 0 1 0.12 0 0
CUI: C1865433
Disease: VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF
VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF 		1 0 1 0.12 0 0
CUI: C1865553
Disease: HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO
HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO 		1 0 1 0.12 0 0
CUI: C1969371
Disease: Impaired renal uric acid clearance
Impaired renal uric acid clearance 		1 0 1 0.12 0 0
CUI: C2750893
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11 		1 0 1 0.12 0 0
CUI: C3278154
Disease: GLUTARIC ACIDEMIA IIA
GLUTARIC ACIDEMIA IIA 		1 0 1 0.12 0 0