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: C4025698
Disease: Abnormality of the peritoneum
Abnormality of the peritoneum 		9 0 2 8.3E-02 0 0
CUI: C0020440
Disease: Hypercapnia
Hypercapnia 		11 0 2 7.7E-02 0 0
CUI: C3714580
Disease: Hypokalemic periodic paralysis type 1
Hypokalemic periodic paralysis type 1 		12 0 2 7.4E-02 0 0
CUI: C4022395
Disease: Abnormality of the mediastinum
Abnormality of the mediastinum 		12 0 2 7.4E-02 0 0
CUI: C4020730
Disease: Increased intramyocellular lipid droplets
Increased intramyocellular lipid droplets 		27 0 3 7.3E-02 0 0
CUI: C0041657
Disease: Unconscious State
Unconscious State 		13 0 2 7.1E-02 0 0
CUI: C0042258
Disease: Vaginal Neoplasms
Vaginal Neoplasms 		13 0 2 7.1E-02 0 0
CUI: C0268059
Disease: Neonatal hemochromatosis
Neonatal hemochromatosis 		13 0 2 7.1E-02 0 0
CUI: C1846288
Disease: Recurrent hypoglycemia
Recurrent hypoglycemia 		13 0 2 7.1E-02 0 0
CUI: C4025663
Disease: Abnormality of tibia morphology
Abnormality of tibia morphology 		13 2 2 7.1E-02 2 0.50
CUI: C0021141
Disease: Inappropriate ADH Syndrome
Inappropriate ADH Syndrome 		14 1 2 6.9E-02 1 0.25
CUI: C0266316
Disease: Congenital hydronephrosis
Congenital hydronephrosis 		15 0 2 6.7E-02 0 0
CUI: C0020461
Disease: Hyperkalemia
Hyperkalemia 		32 0 3 6.5E-02 0 0
CUI: C0028081
Disease: Night sweats
Night sweats 		17 0 2 6.2E-02 0 0
CUI: C0235259
Disease: Subcapsular cataract
Subcapsular cataract 		17 0 2 6.2E-02 0 0
CUI: C3665335
Disease: Cutis laxa, autosomal recessive
Cutis laxa, autosomal recessive 		17 0 2 6.2E-02 0 0
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		18 0 2 6.1E-02 0 0
CUI: C1279412
Disease: periodic paralysis (finding)
periodic paralysis (finding) 		18 0 2 6.1E-02 0 0
CUI: C0035410
Disease: Rhabdomyolysis
Rhabdomyolysis 		36 0 3 6.0E-02 0 0
CUI: C0001889
Disease: Akinetic Mutism
Akinetic Mutism 		1 0 1 5.9E-02 0 0
CUI: C0015263
Disease: Bronchospasm, Exercise-Induced
Bronchospasm, Exercise-Induced 		1 0 1 5.9E-02 0 0
CUI: C0022802
Disease: Kuru
Kuru 		1 0 1 5.9E-02 0 0
CUI: C0025467
Disease: Mesenteric Cyst
Mesenteric Cyst 		1 2 1 5.9E-02 2 0.50
CUI: C0025988
Disease: Microglossia
Microglossia 		19 0 2 5.9E-02 0 0
CUI: C0037942
Disease: Spinal Osteophytosis
Spinal Osteophytosis 		1 0 1 5.9E-02 0 0