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: C0011880
Disease: Diabetic Ketoacidosis
Diabetic Ketoacidosis 		63 0 8 6.9E-02 0 0
CUI: C0020649
Disease: Hypotension
Hypotension 		125 0 12 6.9E-02 0 0
CUI: C0010481
Disease: Cushing Syndrome
Cushing Syndrome 		126 0 12 6.9E-02 0 0
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism 		50 0 7 6.7E-02 0 0
CUI: C0020428
Disease: Hyperaldosteronism
Hyperaldosteronism 		84 0 9 6.6E-02 0 0
CUI: C0549622
Disease: Sexual Dysfunction
Sexual Dysfunction 		36 12 6 6.6E-02 1 6.2E-02
CUI: C0809983
Disease: Schizophrenia and related disorders
Schizophrenia and related disorders 		20 0 5 6.6E-02 0 0
CUI: C4703616
Disease: Decreased level of 1,5 anhydroglucitol in serum
Decreased level of 1,5 anhydroglucitol in serum 		4 0 4 6.6E-02 0 0
CUI: C0232831
Disease: Impairment of urinary concentration
Impairment of urinary concentration 		5 0 4 6.5E-02 0 0
CUI: C4021038
Disease: Abnormal circulating renin
Abnormal circulating renin 		5 0 4 6.5E-02 0 0
CUI: C1846347
Disease: Renal salt wasting
Renal salt wasting 		22 0 5 6.4E-02 0 0
CUI: C0039231
Disease: Tachycardia
Tachycardia 		73 0 8 6.3E-02 0 0
CUI: C1846348
Disease: Renal potassium wasting
Renal potassium wasting 		6 0 4 6.3E-02 0 0
CUI: C0009777
Disease: Conn Adenoma
Conn Adenoma 		107 0 10 6.3E-02 0 0
CUI: C0039621
Disease: Tetany
Tetany 		24 0 5 6.2E-02 0 0
CUI: C1522135
Disease: Hypermagnesemia result
Hypermagnesemia result 		7 0 4 6.2E-02 0 0
CUI: C4554647
Disease: Hypermagnesemia, CTCAE
Hypermagnesemia, CTCAE 		7 0 4 6.2E-02 0 0
CUI: C0086769
Disease: Panic Attacks
Panic Attacks 		59 0 7 6.2E-02 0 0
CUI: C1968619
Disease: Renal corticomedullary cysts
Renal corticomedullary cysts 		8 0 4 6.2E-02 0 0
CUI: C1960870
Disease: Transformed migraine
Transformed migraine 		43 0 6 6.1E-02 0 0
CUI: C4021551
Disease: Absence of secondary sex characteristics
Absence of secondary sex characteristics 		44 0 6 6.1E-02 0 0
CUI: C4551693
Disease: Wolfram Syndrome 1
Wolfram Syndrome 1 		9 0 4 6.1E-02 0 0
CUI: C0151714
Disease: Hypermagnesemia
Hypermagnesemia 		10 0 4 6.0E-02 0 0
CUI: C0266444
Disease: Congenital absence of vas deferens
Congenital absence of vas deferens 		10 0 4 6.0E-02 0 0
CUI: C1835171
Disease: Hypomagnesemia 2, renal
Hypomagnesemia 2, renal 		10 0 4 6.0E-02 0 0