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: C4022766
Disease: Abnormal large intestine physiology
Abnormal large intestine physiology 		3 0 3 1.00 0 0
CUI: C4023764
Disease: Elevated alkaline phosphatase of hepatic origin
Elevated alkaline phosphatase of hepatic origin 		3 0 3 1.00 0 0
CUI: C4022867
Disease: Spider hemangioma
Spider hemangioma 		4 0 3 0.75 0 0
CUI: C4020948
Disease: Palmar telangiectasia
Palmar telangiectasia 		5 0 3 0.60 0 0
CUI: C4025612
Disease: Polyclonal elevation of IgM
Polyclonal elevation of IgM 		5 0 3 0.60 0 0
CUI: C2750451
Disease: CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3 		1 0 1 0.33 0 0
CUI: C1839765
Disease: Triangular nasal tip
Triangular nasal tip 		2 0 1 0.25 0 0
CUI: C0426430
Disease: Drooping nasal tip
Drooping nasal tip 		3 0 1 0.20 0 0
CUI: C1828017
Disease: Intermittent hyperventilation
Intermittent hyperventilation 		3 0 1 0.20 0 0
CUI: C1850959
Disease: Corneal dystrophy, Fuchs' endothelial, 1
Corneal dystrophy, Fuchs' endothelial, 1 		9 0 2 0.20 0 0
CUI: C1968816
Disease: Broad fingertip
Broad fingertip 		3 0 1 0.20 0 0
CUI: C4024917
Disease: Congenital encephalopathy
Congenital encephalopathy 		3 0 1 0.20 0 0
CUI: C4025056
Disease: Failure of eruption of permanent teeth
Failure of eruption of permanent teeth 		5 0 1 0.14 0 0
CUI: C0576227
Disease: Narrow foot
Narrow foot 		6 0 1 0.12 0 0
CUI: C1857800
Disease: CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2 		6 0 1 0.12 0 0
CUI: C2936476
Disease: Chronic Liver Failure
Chronic Liver Failure 		25 0 3 0.12 0 0
CUI: C0264009
Disease: Osteodystrophy
Osteodystrophy 		7 0 1 0.11 0 0
CUI: C4054912
Disease: Fusion-Positive Alveolar Rhabdomyosarcoma
Fusion-Positive Alveolar Rhabdomyosarcoma 		7 0 1 0.11 0 0
CUI: C0151872
Disease: Prothrombin time increased
Prothrombin time increased 		30 0 3 1.0E-01 0 0
CUI: C1837503
Disease: Small cerebral cortex
Small cerebral cortex 		8 0 1 1.0E-01 0 0
CUI: C3553943
Disease: T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS
T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS 		8 0 1 1.0E-01 0 0
CUI: C3891556
Disease: CHROMOSOME Xq26.3 DUPLICATION SYNDROME
CHROMOSOME Xq26.3 DUPLICATION SYNDROME 		8 0 1 1.0E-01 0 0
CUI: C4225671
Disease: VATER/VACTERL ASSOCIATION
VATER/VACTERL ASSOCIATION 		8 0 1 1.0E-01 0 0
CUI: C4551951
Disease: Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		8 0 1 1.0E-01 0 0
CUI: C1562061
Disease: Microspherophakia
Microspherophakia 		9 0 1 9.1E-02 0 0