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: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY
18 37 18 1.00 0 37 1.00 0
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome
4 5 3 0.16 0 1 2.4E-02 3.0E-03
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
15 26 4 0.14 0 2 3.3E-02 0
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
15 26 4 0.14 0 2 3.3E-02 0
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
15 26 4 0.14 0 2 3.3E-02 0
Leigh Syndrome due to Mitochondrial Complex III Deficiency
15 26 4 0.14 0 2 3.3E-02 0
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
15 26 4 0.14 0 2 3.3E-02 0
Leigh Syndrome due to Mitochondrial Complex V Deficiency
15 26 4 0.14 0 2 3.3E-02 0
Necrotizing encephalopathy, infantile subacute, of Leigh
15 26 4 0.14 0 2 3.3E-02 0
CUI: C0917796
Disease: Optic Atrophy, Hereditary, Leber
Optic Atrophy, Hereditary, Leber
9 22 3 0.12 0 0 0
ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL
2 1 1 5.3E-02 1.0E-02 0 0
CUI: C1839040
Disease: LEBER OPTIC ATROPHY AND DYSTONIA
LEBER OPTIC ATROPHY AND DYSTONIA
2 3 1 5.3E-02 1.0E-02 1 2.6E-02 1.0E-03
CUI: C1527249
Disease: Colorectal Cancer
Colorectal Cancer
459 294 1 2.1E-03 0.89 0 0