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: C0234458
Disease: Dream disorder
Dream disorder 		1 0 1 0.50 0 0
CUI: C0458118
Disease: Total body pain syndrome
Total body pain syndrome 		1 0 1 0.50 0 0
CUI: C0862953
Disease: Cholangiocarcinoma non-resectable
Cholangiocarcinoma non-resectable 		1 0 1 0.50 0 0
CUI: C1274408
Disease: Chronic plaque-like oral candidiasis
Chronic plaque-like oral candidiasis 		1 0 1 0.50 0 0
CUI: C1306229
Disease: Dyschromatosis universalis
Dyschromatosis universalis 		1 0 1 0.50 0 0
CUI: C1836705
Disease: Pseudohyperkalemia, Familial, 2, due to Red Cell Leak
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak 		1 0 1 0.50 0 0
CUI: C3809394
Disease: DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3 		1 0 1 0.50 0 0
CUI: C4016851
Disease: BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY
BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY 		1 0 1 0.50 0 0
CUI: C4025631
Disease: Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes
Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes 		1 0 1 0.50 0 0
CUI: C4273970
Disease: Familial pseudohyperkalemia
Familial pseudohyperkalemia 		1 0 1 0.50 0 0
CUI: C0919785
Disease: Decreased transferrin saturation
Decreased transferrin saturation 		2 0 1 0.33 0 0
CUI: C1851943
Disease: DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT (disorder)
DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT (disorder) 		2 0 1 0.33 0 0
CUI: C1860315
Disease: Whispering dysphonia, hereditary
Whispering dysphonia, hereditary 		2 0 1 0.33 0 0
CUI: C1963899
Disease: Erosive gastroduodenitis
Erosive gastroduodenitis 		2 0 1 0.33 0 0
CUI: C2919706
Disease: Idiopathic rapidly progressive glomerulonephritis
Idiopathic rapidly progressive glomerulonephritis 		2 0 1 0.33 0 0
CUI: C3541471
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1 		2 13 1 0.33 3 8.1E-02
CUI: C4025022
Disease: Decreased mitochondrial complex III activity in liver tissue
Decreased mitochondrial complex III activity in liver tissue 		2 0 1 0.33 0 0
CUI: C1565249
Disease: Mobility Limitation
Mobility Limitation 		3 0 1 0.25 0 0
CUI: C1859372
Disease: Calcification of Joints and Arteries
Calcification of Joints and Arteries 		3 0 1 0.25 0 0
CUI: C3281027
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7 		3 0 1 0.25 0 0
CUI: C1839437
Disease: Chronic lactic acidosis
Chronic lactic acidosis 		4 0 1 0.20 0 0
CUI: C1859495
Disease: Episodic hemolytic anemia
Episodic hemolytic anemia 		4 0 1 0.20 0 0
CUI: C0268344
Disease: Ehlers-Danlos syndrome 6B
Ehlers-Danlos syndrome 6B 		5 0 1 0.17 0 0
CUI: C0344516
Disease: Coloboma of lens
Coloboma of lens 		5 0 1 0.17 0 0
CUI: C0542141
Disease: Paralysis radial
Paralysis radial 		5 0 1 0.17 0 0