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: C0337443
Disease: Sodium measurement
Sodium measurement 		53 69 8 0.13 5 6.0E-02
CUI: C2675866
Disease: DIABETES MELLITUS, INSULIN-DEPENDENT, 20 (disorder)
DIABETES MELLITUS, INSULIN-DEPENDENT, 20 (disorder) 		2 0 2 0.12 0 0
CUI: C0202194
Disease: Potassium measurement
Potassium measurement 		16 28 3 0.10 2 4.4E-02
CUI: C0342277
Disease: Diabetes mellitus autosomal dominant type II (disorder)
Diabetes mellitus autosomal dominant type II (disorder) 		8 139 2 9.1E-02 1 6.4E-03
CUI: C1838100
Disease: MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder)
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder) 		12 0 2 7.7E-02 0 0
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		1 0 1 6.2E-02 0 0
CUI: C1840646
Disease: Hepatic Adenomas, Familial
Hepatic Adenomas, Familial 		1 0 1 6.2E-02 0 0
CUI: C2750771
Disease: Amelogenesis Imperfecta, Hypomaturation Type, Iia3
Amelogenesis Imperfecta, Hypomaturation Type, Iia3 		1 0 1 6.2E-02 0 0
CUI: C3150714
Disease: FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5 		1 0 1 6.2E-02 0 0
CUI: C3890591
Disease: NEPHRONOPHTHISIS 18
NEPHRONOPHTHISIS 18 		1 0 1 6.2E-02 0 0
CUI: C4021748
Disease: Abnormal B cell morphology
Abnormal B cell morphology 		1 0 1 6.2E-02 0 0
CUI: C4023540
Disease: Hypomature dental enamel
Hypomature dental enamel 		1 0 1 6.2E-02 0 0
CUI: C4054588
Disease: Lymphocytic Neurohypophysitis
Lymphocytic Neurohypophysitis 		1 0 1 6.2E-02 0 0
CUI: C4273658
Disease: Graham Little Piccardi Lassueur syndrome
Graham Little Piccardi Lassueur syndrome 		1 0 1 6.2E-02 0 0
CUI: C4303475
Disease: Hyperinsulinism due to HNF1A deficiency
Hyperinsulinism due to HNF1A deficiency 		1 0 1 6.2E-02 0 0
CUI: C4748341
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67 		1 0 1 6.2E-02 0 0
CUI: C4748364
Disease: USHER SYNDROME, TYPE IV
USHER SYNDROME, TYPE IV 		1 0 1 6.2E-02 0 0
CUI: C4748741
Disease: VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION
VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION 		1 0 1 6.2E-02 0 0
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		54 108 4 6.1E-02 2 1.6E-02
CUI: C0403502
Disease: Low renal threshold for glucose
Low renal threshold for glucose 		2 0 1 5.9E-02 0 0
CUI: C1846059
Disease: Roifman syndrome
Roifman syndrome 		2 0 1 5.9E-02 0 0
CUI: C1969038
Disease: RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)
RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder) 		2 0 1 5.9E-02 0 0
CUI: C1969807
Disease: Dystonia, Focal, Task-Specific
Dystonia, Focal, Task-Specific 		2 0 1 5.9E-02 0 0
CUI: C2749929
Disease: Musician's Dystonia
Musician's Dystonia 		2 0 1 5.9E-02 0 0
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		39 568 3 5.8E-02 1 1.7E-03