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: C1866021
Disease: Increased connective tissue
Increased connective tissue 		16 0 1 6.2E-02 0 0
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		5725 0 1 1.7E-04 0 0
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection 		695 0 1 1.4E-03 0 0
CUI: C3148763
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E 		4 0 1 0.25 0 0
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
Human immunodeficiency virus (HIV) II infection category B1 		985 0 1 1.0E-03 0 0
CUI: C4013182
Disease: Caused by mutation in the transportin 3 gene (TNPO3, 610032.0001)
Caused by mutation in the transportin 3 gene (TNPO3, 610032.0001) 		1 0 1 1.00 0 0
CUI: C4021768
Disease: Abnormality of metabolism/homeostasis
Abnormality of metabolism/homeostasis 		171 0 1 5.8E-03 0 0
CUI: C4023577
Disease: Abnormality of the intrahepatic bile duct
Abnormality of the intrahepatic bile duct 		10 0 1 1.0E-01 0 0
CUI: C4025565
Disease: Late-onset distal muscle weakness
Late-onset distal muscle weakness 		3 0 1 0.33 0 0
CUI: C4317107
Disease: Abnormality of the thyroid gland
Abnormality of the thyroid gland 		21 0 1 4.8E-02 0 0
CUI: C0427064
Disease: Pelvic girdle weakness
Pelvic girdle weakness 		16 2 1 6.2E-02 1 0.25
CUI: C0560346
Disease: Difficulty running
Difficulty running 		38 3 1 2.6E-02 1 0.20
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness 		39 4 1 2.6E-02 1 0.17
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 16 1 8.7E-03 1 5.6E-02
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		280 67 1 3.6E-03 1 1.4E-02