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: C0023380
Disease: Lethargy
Lethargy
160 0 83 0.22 0 0
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia
420 0 99 0.16 0 0
CUI: C0027497
Disease: Nausea
Nausea
161 14 63 0.16 4 0.12
CUI: C0011991
Disease: Diarrhea
Diarrhea
632 63 117 0.14 1 1.2E-02
CUI: C0009421
Disease: Comatose
Comatose
78 0 45 0.13 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
842 0 133 0.13 0 0
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
523 0 94 0.13 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 18 67 0.12 3 7.9E-02
CUI: C0003123
Disease: Anorexia
Anorexia
242 0 56 0.11 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
209 0 52 0.11 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy
37 0 34 0.11 0 0
CUI: C0220994
Disease: Hyperammonemia
Hyperammonemia
102 0 40 0.11 0 0
CUI: C0027498
Disease: Nausea and vomiting
Nausea and vomiting
257 11 55 0.11 1 3.0E-02
CUI: C0022638
Disease: Ketosis
Ketosis
119 0 40 0.10 0 0
CUI: C0020625
Disease: Hyponatremia
Hyponatremia
109 11 37 9.9E-02 1 3.0E-02
CUI: C0085584
Disease: Encephalopathies
Encephalopathies
457 0 68 9.8E-02 0 0
CUI: C0009806
Disease: Constipation
Constipation
424 57 65 9.8E-02 3 3.9E-02
CUI: C4721453
Disease: Peripheral Nervous System Diseases
Peripheral Nervous System Diseases
549 69 76 9.8E-02 1 1.1E-02
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies
121 0 37 9.6E-02 0 0
CUI: C0018681
Disease: Headache
Headache
338 0 55 9.4E-02 0 0
CUI: C0085605
Disease: Liver Failure
Liver Failure
293 0 51 9.4E-02 0 0
Decreased activity of mitochondrial complex I
41 0 29 9.2E-02 0 0
CUI: C0020649
Disease: Hypotension
Hypotension
125 0 36 9.2E-02 0 0
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
473 62 65 9.1E-02 1 1.2E-02
CUI: C0015930
Disease: Fetal Distress
Fetal Distress
44 0 29 9.1E-02 0 0