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: C4538570
Disease: COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY
COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY 		3 0 2 0.33 0 0
CUI: C0019050
Disease: Hemoglobinuria, Paroxysmal
Hemoglobinuria, Paroxysmal 		9 0 3 0.27 0 0
CUI: C0020800
Disease: Idiopathic Hypercatabolic Hypoproteinemia
Idiopathic Hypercatabolic Hypoproteinemia 		1 0 1 0.20 0 0
CUI: C0423772
Disease: Cutaneous Fistula
Cutaneous Fistula 		1 0 1 0.20 0 0
CUI: C1263777
Disease: Neoplasm of body of uterus
Neoplasm of body of uterus 		1 0 1 0.20 0 0
CUI: C3275508
Disease: MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2
MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2 		1 0 1 0.20 0 0
CUI: C3806670
Disease: PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1 		1 0 1 0.20 0 0
CUI: C4025198
Disease: Recurrent gram-negative bacterial infections
Recurrent gram-negative bacterial infections 		1 0 1 0.20 0 0
CUI: C4510605
Disease: Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency 		1 0 1 0.20 0 0
CUI: C4531045
Disease: Reduced granulocyte CD59 level
Reduced granulocyte CD59 level 		1 0 1 0.20 0 0
CUI: C4540531
Disease: CROMER BLOOD GROUP SYSTEM, Dr(a-) PHENOTYPE
CROMER BLOOD GROUP SYSTEM, Dr(a-) PHENOTYPE 		1 0 1 0.20 0 0
CUI: C4751570
Disease: Ferro-cerebro-cutaneous syndrome
Ferro-cerebro-cutaneous syndrome 		1 0 1 0.20 0 0
CUI: C4755276
Disease: Primary CD59 deficiency
Primary CD59 deficiency 		1 0 1 0.20 0 0
CUI: C0023510
Disease: Leukocyte Disorders
Leukocyte Disorders 		2 0 1 0.17 0 0
CUI: C0039010
Disease: Swine Vesicular Disease
Swine Vesicular Disease 		2 0 1 0.17 0 0
CUI: C0086774
Disease: Cold paroxysmal hemoglobinuria
Cold paroxysmal hemoglobinuria 		2 0 1 0.17 0 0
CUI: C0267372
Disease: Primary intestinal lymphangiectasia
Primary intestinal lymphangiectasia 		2 0 1 0.17 0 0
CUI: C1846175
Disease: SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder)
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder) 		2 0 1 0.17 0 0
CUI: C2936826
Disease: Fumaric aciduria
Fumaric aciduria 		2 0 1 0.17 0 0
CUI: C4024862
Disease: Recurrent staphylococcal infections
Recurrent staphylococcal infections 		2 0 1 0.17 0 0
CUI: C0340319
Disease: Posterior myocardial infarction
Posterior myocardial infarction 		3 0 1 0.14 0 0
CUI: C1504438
Disease: Cerebral artery stenosis
Cerebral artery stenosis 		3 0 1 0.14 0 0
CUI: C4087338
Disease: Mite allergy
Mite allergy 		3 0 1 0.14 0 0
CUI: C0264695
Disease: Subendocardial ischemia
Subendocardial ischemia 		4 0 1 0.12 0 0
CUI: C1504514
Disease: Infection by human herpesvirus 7
Infection by human herpesvirus 7 		4 0 1 0.12 0 0