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: C0020626
Disease: Hypoparathyroidism
Hypoparathyroidism
92 0 30 0.10 0 0
CUI: C1519353
Disease: Skin Papule
Skin Papule
74 0 28 0.10 0 0
CUI: C0018681
Disease: Headache
Headache
338 75 52 0.10 1 1.0E-02
CUI: C0034150
Disease: Purpura
Purpura
68 0 27 0.10 0 0
CUI: C0702166
Disease: Acne
Acne
167 0 36 0.10 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers
59 0 26 0.10 0 0
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
345 0 52 0.10 0 0
CUI: C0009806
Disease: Constipation
Constipation
424 0 59 1.0E-01 0 0
CUI: C0031046
Disease: Pericarditis
Pericarditis
51 0 25 9.9E-02 0 0
CUI: C0542476
Disease: Forgetful
Forgetful
429 0 59 9.9E-02 0 0
CUI: C2937365
Disease: Recurrent aphthous ulcer
Recurrent aphthous ulcer
80 0 27 9.7E-02 0 0
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency
615 42 74 9.6E-02 1 1.6E-02
CUI: C0151311
Disease: Cranial nerve palsies
Cranial nerve palsies
81 0 27 9.6E-02 0 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
175 0 35 9.6E-02 0 0
CUI: C3714745
Disease: Malabsorption
Malabsorption
175 0 35 9.6E-02 0 0
CUI: C0006625
Disease: Cachexia
Cachexia
273 0 43 9.4E-02 0 0
CUI: C0024523
Disease: Malabsorption Syndrome
Malabsorption Syndrome
239 0 40 9.4E-02 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities
115 0 29 9.3E-02 0 0
CUI: C0017086
Disease: Gangrene
Gangrene
69 0 25 9.3E-02 0 0
CUI: C0234428
Disease: Disturbance of consciousness
Disturbance of consciousness
35 0 22 9.2E-02 0 0
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency
315 0 45 9.1E-02 0 0
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
403 0 52 9.0E-02 0 0
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
502 0 60 9.0E-02 0 0
CUI: C0019079
Disease: Hemoptysis
Hemoptysis
67 0 24 8.9E-02 0 0
CUI: C0086543
Disease: Cataract
Cataract
878 0 90 8.9E-02 0 0