Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
51 0 1 1.9E-03 0 0
CUI: C0856727
Disease: Cholesterol gallstones
Cholesterol gallstones
51 0 1 1.9E-03 0 0
Chronic progressive external ophthalmoplegia
50 0 1 1.9E-03 0 0
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders
50 0 1 1.9E-03 0 0
Increased variability in muscle fiber diameter
50 0 1 1.9E-03 0 0
CUI: C0730362
Disease: Disorder of macula of retina
Disorder of macula of retina
49 0 1 1.9E-03 0 0
CUI: C2609129
Disease: Autoimmune pancreatitis
Autoimmune pancreatitis
49 0 1 1.9E-03 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy
48 0 1 1.9E-03 0 0
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive
48 0 1 1.9E-03 0 0
Congenital hypoplasia of adrenal gland
45 0 1 1.9E-03 0 0
CUI: C1849488
Disease: Increased serum pyruvate
Increased serum pyruvate
45 0 1 1.9E-03 0 0
CUI: C0240421
Disease: Progressive muscle weakness
Progressive muscle weakness
44 0 1 1.9E-03 0 0
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
44 0 1 1.9E-03 0 0
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting
43 0 1 1.9E-03 0 0
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus
42 0 1 1.9E-03 0 0
Thyroid stimulating hormone measurement
42 0 1 1.9E-03 0 0
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease
42 0 1 1.9E-03 0 0
Adverse Event Associated with Cardiac Arrhythmia
42 0 1 1.9E-03 0 0
CUI: C0231921
Disease: Pulmonary function
Pulmonary function
41 0 1 1.9E-03 0 0
CUI: C0272178
Disease: Drug-induced neutropenia
Drug-induced neutropenia
41 0 1 1.9E-03 0 0
CUI: C0858600
Disease: Taste sweet
Taste sweet
41 0 1 1.9E-03 0 0
Decreased activity of mitochondrial complex I
41 0 1 1.9E-03 0 0
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding)
41 0 1 1.9E-03 0 0
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder)
40 0 1 2.0E-03 0 0
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
40 0 1 2.0E-03 0 0