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: C3151513
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)
MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE) 		1 0 1 1.00 0 0
CUI: C4025018
Disease: Depletion of mitochondrial DNA in liver
Depletion of mitochondrial DNA in liver 		1 0 1 1.00 0 0
CUI: C4025595
Disease: Viral infection-induced rhabdomyolysis
Viral infection-induced rhabdomyolysis 		1 0 1 1.00 0 0
CUI: C4310733
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4 		1 7 1 1.00 1 0.12
CUI: C0220993
Disease: Cystathioninuria
Cystathioninuria 		2 0 1 0.50 0 0
CUI: C4310735
Disease: PORTAL HYPERTENSION, NONCIRRHOTIC
PORTAL HYPERTENSION, NONCIRRHOTIC 		2 2 1 0.50 1 0.33
CUI: C0010398
Disease: Cruveilhier-Baumgarten Syndrome
Cruveilhier-Baumgarten Syndrome 		4 0 1 0.25 0 0
CUI: C1328348
Disease: Mitochondrial hepatopathy
Mitochondrial hepatopathy 		4 0 1 0.25 0 0
CUI: C1849766
Disease: Periportal fibrosis
Periportal fibrosis 		4 0 1 0.25 0 0
CUI: C3711385
Disease: Deoxyguanosine Kinase Deficiency
Deoxyguanosine Kinase Deficiency 		4 0 1 0.25 0 0
CUI: C0268616
Disease: Gamma-cystathionase deficiency
Gamma-cystathionase deficiency 		5 0 1 0.20 0 0
CUI: C1845274
Disease: Abnormal conjugate eye movement
Abnormal conjugate eye movement 		7 0 1 0.14 0 0
CUI: C1842552
Disease: Limb-girdle muscle atrophy
Limb-girdle muscle atrophy 		8 0 1 0.12 0 0
CUI: C4021534
Disease: Adult onset sensorineural hearing impairment
Adult onset sensorineural hearing impairment 		8 0 1 0.12 0 0
CUI: C0240595
Disease: Rotary Nystagmus
Rotary Nystagmus 		9 0 1 0.11 0 0
CUI: C1847868
Disease: Generalized aminoaciduria
Generalized aminoaciduria 		11 0 1 9.1E-02 0 0
CUI: C0004093
Disease: Asthenia
Asthenia 		16 0 1 6.2E-02 0 0
CUI: C0427064
Disease: Pelvic girdle weakness
Pelvic girdle weakness 		16 0 1 6.2E-02 0 0
CUI: C0267812
Disease: Micronodular cirrhosis
Micronodular cirrhosis 		18 0 1 5.6E-02 0 0
CUI: C1842587
Disease: Sensory axonal neuropathy
Sensory axonal neuropathy 		23 0 1 4.3E-02 0 0
CUI: C0205710
Disease: Alpers Syndrome (disorder)
Alpers Syndrome (disorder) 		28 0 1 3.6E-02 0 0
CUI: C4024609
Disease: Decreased activity of mitochondrial respiratory chain
Decreased activity of mitochondrial respiratory chain 		34 0 1 2.9E-02 0 0
CUI: C0342782
Disease: Depletion of mitochondrial DNA
Depletion of mitochondrial DNA 		36 0 1 2.8E-02 0 0
CUI: C1855038
Disease: Hepatocellular necrosis
Hepatocellular necrosis 		41 0 1 2.4E-02 0 0
CUI: C0949857
Disease: Mitochondrial Respiratory Chain Deficiencies
Mitochondrial Respiratory Chain Deficiencies 		49 0 1 2.0E-02 0 0