Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
21 24 6 8.0E-02 1 3.1E-02
CUI: C1868773
Disease: Diabetic encephalopathy
Diabetic encephalopathy
21 0 6 8.0E-02 0 0
CUI: C0426870
Disease: Large hand
Large hand
35 0 7 8.0E-02 0 0
CUI: C0346326
Disease: Optic Nerve Glioma
Optic Nerve Glioma
22 0 6 7.9E-02 0 0
CUI: C0266619
Disease: Potter's facies
Potter's facies
9 0 5 7.8E-02 0 0
CUI: C1850830
Disease: Exercise-induced myalgia
Exercise-induced myalgia
37 0 7 7.8E-02 0 0
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia
176 0 17 7.8E-02 0 0
CUI: C0033141
Disease: Cardiomyopathies, Primary
Cardiomyopathies, Primary
108 0 12 7.7E-02 0 0
CUI: C0334348
Disease: Hidradenoma Papilliferum
Hidradenoma Papilliferum
10 0 5 7.7E-02 0 0
CUI: C0472390
Disease: High altitude cerebral edema
High altitude cerebral edema
10 0 5 7.7E-02 0 0
CUI: C3495831
Disease: Aluminium overload
Aluminium overload
10 0 5 7.7E-02 0 0
CUI: C1560305
Disease: Prolonged QTc interval
Prolonged QTc interval
25 0 6 7.6E-02 0 0
CUI: C1963217
Disease: Prolonged QTc Interval, CTCAE
Prolonged QTc Interval, CTCAE
25 0 6 7.6E-02 0 0
Arrhythmogenic Right Ventricular Dysplasia
82 0 10 7.6E-02 0 0
CUI: C0020503
Disease: Hyperparathyroidism, Secondary
Hyperparathyroidism, Secondary
68 0 9 7.6E-02 0 0
CUI: C1695782
Disease: Cerebral hypoperfusion
Cerebral hypoperfusion
40 0 7 7.5E-02 0 0
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy
226 0 20 7.5E-02 0 0
CUI: C1858025
Disease: Spinal rigidity
Spinal rigidity
55 0 8 7.5E-02 0 0
CUI: C0151718
Disease: Hypocholesterolemia
Hypocholesterolemia
113 0 12 7.5E-02 0 0
Left ventricular systolic dysfunction
41 0 7 7.4E-02 0 0
CUI: C1842060
Disease: Prominent supraorbital ridges
Prominent supraorbital ridges
41 0 7 7.4E-02 0 0
CUI: C0013390
Disease: Dysmenorrhea
Dysmenorrhea
71 0 9 7.4E-02 0 0
CUI: C0162770
Disease: Right Ventricular Hypertrophy
Right Ventricular Hypertrophy
160 0 15 7.3E-02 0 0
Progressive proximal muscle weakness
28 0 6 7.3E-02 0 0
CUI: C4522181
Disease: Brachial Amyotrophic Diplegia
Brachial Amyotrophic Diplegia
28 0 6 7.3E-02 0 0