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: C0155002
Disease: Sudden visual loss
Sudden visual loss 		1 0 1 0.50 0 0
CUI: C3151513
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)
MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE) 		1 12 1 0.50 1 7.7E-02
CUI: C4025018
Disease: Depletion of mitochondrial DNA in liver
Depletion of mitochondrial DNA in liver 		1 0 1 0.50 0 0
CUI: C4025595
Disease: Viral infection-induced rhabdomyolysis
Viral infection-induced rhabdomyolysis 		1 0 1 0.50 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 0.50 2 0.29
CUI: C4310935
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 3
MITOCHONDRIAL DNA DEPLETION SYNDROME 3 		1 2 1 0.50 1 0.33
CUI: C0220993
Disease: Cystathioninuria
Cystathioninuria 		2 0 1 0.33 0 0
CUI: C0010398
Disease: Cruveilhier-Baumgarten Syndrome
Cruveilhier-Baumgarten Syndrome 		4 0 1 0.20 0 0
CUI: C1328348
Disease: Mitochondrial hepatopathy
Mitochondrial hepatopathy 		4 0 1 0.20 0 0
CUI: C1849766
Disease: Periportal fibrosis
Periportal fibrosis 		4 0 1 0.20 0 0
CUI: C3711385
Disease: Deoxyguanosine Kinase Deficiency
Deoxyguanosine Kinase Deficiency 		4 0 1 0.20 0 0
CUI: C0268616
Disease: Gamma-cystathionase deficiency
Gamma-cystathionase deficiency 		5 0 1 0.17 0 0
CUI: C1859896
Disease: Progressive macrocephaly
Progressive macrocephaly 		5 0 1 0.17 0 0
CUI: C0004093
Disease: Asthenia
Asthenia 		16 0 2 0.12 0 0
CUI: C1845274
Disease: Abnormal conjugate eye movement
Abnormal conjugate eye movement 		7 0 1 0.12 0 0
CUI: C1842552
Disease: Limb-girdle muscle atrophy
Limb-girdle muscle atrophy 		8 0 1 0.11 0 0
CUI: C1855020
Disease: Acute necrotizing encephalopathy
Acute necrotizing encephalopathy 		8 0 1 0.11 0 0
CUI: C4021534
Disease: Adult onset sensorineural hearing impairment
Adult onset sensorineural hearing impairment 		8 0 1 0.11 0 0
CUI: C0240595
Disease: Rotary Nystagmus
Rotary Nystagmus 		9 0 1 1.0E-01 0 0
CUI: C0347180
Disease: Penile intraepithelial neoplasia
Penile intraepithelial neoplasia 		9 0 1 1.0E-01 0 0
CUI: C0751267
Disease: Encephalopathy, Subacute Necrotizing, Infantile
Encephalopathy, Subacute Necrotizing, Infantile 		9 0 1 1.0E-01 0 0
CUI: C0751268
Disease: Encephalopathy, Subacute Necrotizing, Juvenile
Encephalopathy, Subacute Necrotizing, Juvenile 		9 0 1 1.0E-01 0 0
CUI: C0239377
Disease: Arm Pain
Arm Pain 		10 0 1 9.1E-02 0 0
CUI: C0729665
Disease: Arteriovenous graft
Arteriovenous graft 		10 0 1 9.1E-02 0 0
CUI: C1847868
Disease: Generalized aminoaciduria
Generalized aminoaciduria 		11 0 1 8.3E-02 0 0