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: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		20 35 20 1.00 35 1.00
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 10 3 0.13 2 4.7E-02
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		6 10 3 0.13 2 4.7E-02
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		26 36 5 0.12 4 6.0E-02
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		17 25 4 0.12 2 3.4E-02
CUI: C0337439
Disease: Iron measurement
Iron measurement 		12 16 3 0.10 1 2.0E-02
CUI: C0428578
Disease: Iron level result
Iron level result 		12 16 3 0.10 1 2.0E-02
CUI: C0036400
Disease: Scimitar Syndrome
Scimitar Syndrome 		2 0 2 1.0E-01 0 0
CUI: C1735886
Disease: Bland White Garland Syndrome
Bland White Garland Syndrome 		2 0 2 1.0E-01 0 0
CUI: C4310699
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24 		2 0 2 1.0E-01 0 0
CUI: C4310700
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44 		2 0 2 1.0E-01 0 0
CUI: C4748946
Disease: CARDIAC-UROGENITAL SYNDROME
CARDIAC-UROGENITAL SYNDROME 		2 0 2 1.0E-01 0 0
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia 		3 0 2 9.5E-02 0 0
CUI: C1456852
Disease: Ventouse delivery (finding)
Ventouse delivery (finding) 		3 0 2 9.5E-02 0 0
CUI: C4021227
Disease: Underdeveloped nasolabial fold
Underdeveloped nasolabial fold 		3 0 2 9.5E-02 0 0
CUI: C4551904
Disease: Total Anomalous Pulmonary Venous Return 1
Total Anomalous Pulmonary Venous Return 1 		3 0 2 9.5E-02 0 0
CUI: C2316832
Disease: Arachidonic acid measurement
Arachidonic acid measurement 		4 0 2 9.1E-02 0 0
CUI: C4025724
Disease: Abnormality of the cerebral ventricles
Abnormality of the cerebral ventricles 		4 0 2 9.1E-02 0 0
CUI: C1858392
Disease: NEPHRONOPHTHISIS 3
NEPHRONOPHTHISIS 3 		6 0 2 8.3E-02 0 0
CUI: C1845274
Disease: Abnormal conjugate eye movement
Abnormal conjugate eye movement 		7 0 2 8.0E-02 0 0
CUI: C1846868
Disease: Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication 		21 0 3 7.9E-02 0 0
CUI: C0344760
Disease: Congenital atresia of mitral valve
Congenital atresia of mitral valve 		8 0 2 7.7E-02 0 0
CUI: C0685707
Disease: Muscular ventricular septum defect
Muscular ventricular septum defect 		9 0 2 7.4E-02 0 0
CUI: C1859347
Disease: Abnormal subcutaneous fat tissue distribution
Abnormal subcutaneous fat tissue distribution 		9 0 2 7.4E-02 0 0
CUI: C4722446
Disease: ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION
ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION 		9 0 2 7.4E-02 0 0