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: C4024751
Disease: Abnormality of the extraocular muscles
Abnormality of the extraocular muscles 		4 0 1 0.20 0 0
CUI: C4551995
Disease: Mitochondrial DNA Depletion Syndrome 1
Mitochondrial DNA Depletion Syndrome 1 		4 0 1 0.20 0 0
CUI: C0004712
Disease: Balo's Concentric Sclerosis
Balo's Concentric Sclerosis 		5 0 1 0.17 0 0
CUI: C0233417
Disease: Poor concentration
Poor concentration 		5 0 1 0.17 0 0
CUI: C1834846
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 		5 0 1 0.17 0 0
CUI: C1849096
Disease: Infantile onset spinocerebellar ataxia
Infantile onset spinocerebellar ataxia 		6 0 1 0.14 0 0
CUI: C1865353
Disease: Ethylmalonic aciduria
Ethylmalonic aciduria 		6 0 1 0.14 0 0
CUI: C3277376
Disease: Multiple mitochondrial DNA deletions
Multiple mitochondrial DNA deletions 		6 0 1 0.14 0 0
CUI: C4020908
Disease: Hypointensity of cerebral white matter on MRI
Hypointensity of cerebral white matter on MRI 		6 0 1 0.14 0 0
CUI: C4025597
Disease: Subsarcolemmal accumulations of abnormally shaped mitochondria
Subsarcolemmal accumulations of abnormally shaped mitochondria 		6 0 1 0.14 0 0
CUI: C4476759
Disease: Stooped posture
Stooped posture 		6 0 1 0.14 0 0
CUI: C0236780
Disease: Mixed bipolar I disorder
Mixed bipolar I disorder 		7 0 1 0.12 0 0
CUI: C0270816
Disease: epilepsy and migraine
epilepsy and migraine 		7 0 1 0.12 0 0
CUI: C0548923
Disease: Burn infection
Burn infection 		7 0 1 0.12 0 0
CUI: C1850848
Disease: Muscle fiber necrosis
Muscle fiber necrosis 		7 0 1 0.12 0 0
CUI: C4021585
Disease: Impaired distal proprioception
Impaired distal proprioception 		7 0 1 0.12 0 0
CUI: C4476705
Disease: Upgaze palsy
Upgaze palsy 		7 0 1 0.12 0 0
CUI: C0264162
Disease: Camptocormia
Camptocormia 		8 0 1 0.11 0 0
CUI: C1842552
Disease: Limb-girdle muscle atrophy
Limb-girdle muscle atrophy 		8 0 1 0.11 0 0
CUI: C3888789
Disease: Pancreatic toxicity
Pancreatic toxicity 		8 0 1 0.11 0 0
CUI: C4021737
Disease: Chromosomal breakage induced by crosslinking agents
Chromosomal breakage induced by crosslinking agents 		8 0 1 0.11 0 0
CUI: C1837256
Disease: Macrovesicular hepatic steatosis
Macrovesicular hepatic steatosis 		9 0 1 1.0E-01 0 0
CUI: C0700078
Disease: Decreased tendon reflex
Decreased tendon reflex 		10 0 1 9.1E-02 0 0
CUI: C0949855
Disease: Electron Transport Chain Deficiencies, Mitochondrial
Electron Transport Chain Deficiencies, Mitochondrial 		10 0 1 9.1E-02 0 0
CUI: C1853767
Disease: Impaired distal vibration sensation
Impaired distal vibration sensation 		10 0 1 9.1E-02 0 0