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: C0151701
Disease: Pulmonary hemorrhage
Pulmonary hemorrhage 		5 0 5 1.00 0 0
CUI: C0264356
Disease: Childhood bronchiectasis
Childhood bronchiectasis 		1 0 1 0.20 0 0
CUI: C0598675
Disease: inborn aminoaciduria
inborn aminoaciduria 		1 0 1 0.20 0 0
CUI: C0856208
Disease: Increased serum zinc
Increased serum zinc 		1 0 1 0.20 0 0
CUI: C1970344
Disease: Congenital Disorder Of Glycosylation, Type IIF
Congenital Disorder Of Glycosylation, Type IIF 		1 0 1 0.20 0 0
CUI: C3671688
Disease: Cyclic Hematopoesis
Cyclic Hematopoesis 		1 0 1 0.20 0 0
CUI: C4016939
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf, MODIFIER OF
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf, MODIFIER OF 		1 0 1 0.20 0 0
CUI: C4049241
Disease: Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency
Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency 		1 0 1 0.20 0 0
CUI: C4072913
Disease: Decreased proportion of memory B cells
Decreased proportion of memory B cells 		1 0 1 0.20 0 0
CUI: C4225334
Disease: AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE
AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE 		1 0 1 0.20 0 0
CUI: C4477009
Disease: Decreased platelet glycoprotein Ib
Decreased platelet glycoprotein Ib 		1 0 1 0.20 0 0
CUI: C0271407
Disease: Synchysis scintillans
Synchysis scintillans 		2 0 1 0.17 0 0
CUI: C1274789
Disease: Ligneous conjunctivitis
Ligneous conjunctivitis 		2 0 1 0.17 0 0
CUI: C1856128
Disease: Hepatic venoocclusive disease with immunodeficiency
Hepatic venoocclusive disease with immunodeficiency 		2 0 1 0.17 0 0
CUI: C4023102
Disease: Elevated plasma citrulline
Elevated plasma citrulline 		2 0 1 0.17 0 0
CUI: C4072899
Disease: Abnormal serum interferon-gamma level
Abnormal serum interferon-gamma level 		2 0 1 0.17 0 0
CUI: C0272175
Disease: Immune neutropenia
Immune neutropenia 		3 0 1 0.14 0 0
CUI: C0743360
Disease: Recurrent ear infections
Recurrent ear infections 		11 0 2 0.14 0 0
CUI: C0855999
Disease: Abnormal eosinophil morphology
Abnormal eosinophil morphology 		3 0 1 0.14 0 0
CUI: C1698818
Disease: Photodamaged skin
Photodamaged skin 		3 0 1 0.14 0 0
CUI: C1968804
Disease: Plasminogen Deficiency, Type I
Plasminogen Deficiency, Type I 		3 0 1 0.14 0 0
CUI: C3839957
Disease: Hereditary cystatin C amyloid angiopathy
Hereditary cystatin C amyloid angiopathy 		3 0 1 0.14 0 0
CUI: C4021036
Disease: Abnormal natural killer cell count
Abnormal natural killer cell count 		3 0 1 0.14 0 0
CUI: C4025602
Disease: Ornithinuria
Ornithinuria 		3 0 1 0.14 0 0
CUI: C4025635
Disease: Argininuria
Argininuria 		3 0 1 0.14 0 0