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: C3276240
Disease: LONG QT SYNDROME 2/3, DIGENIC
LONG QT SYNDROME 2/3, DIGENIC
2 0 2 6.7E-02 0 0
LONG QT SYNDROME 3/6, DIGENIC Disorder
2 0 2 6.7E-02 0 0
LONG QT SYNDROME 1/2, DIGENIC (disorder)
2 6 2 6.7E-02 1 1.7E-02
CUI: C3279093
Disease: LONG QT SYNDROME 2/9, DIGENIC
LONG QT SYNDROME 2/9, DIGENIC
2 0 2 6.7E-02 0 0
Amelogenesis imperfecta nephrocalcinosis
19 0 3 6.5E-02 0 0
CUI: C1865018
Disease: Short QT Syndrome 3
Short QT Syndrome 3
3 0 2 6.5E-02 0 0
CUI: C1865019
Disease: SHORT QT SYNDROME 2 (disorder)
SHORT QT SYNDROME 2 (disorder)
3 9 2 6.5E-02 1 1.6E-02
Catecholaminergic Polymorphic Ventricular Tachycardia Type 1
3 0 2 6.5E-02 0 0
CUI: C0030252
Disease: Palpitations
Palpitations
70 0 6 6.4E-02 0 0
CUI: C1865020
Disease: Short QT Syndrome 1
Short QT Syndrome 1
4 6 2 6.2E-02 1 1.7E-02
CUI: C2678485
Disease: LONG QT SYNDROME 9 (disorder)
LONG QT SYNDROME 9 (disorder)
4 0 2 6.2E-02 0 0
CUI: C3826614
Disease: Cardiac arrest in children
Cardiac arrest in children
4 0 2 6.2E-02 0 0
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block
39 0 4 6.2E-02 0 0
CUI: C0403654
Disease: Bladder outflow obstruction
Bladder outflow obstruction
5 0 2 6.1E-02 0 0
QT interval feature (observable entity)
75 226 6 6.1E-02 3 1.1E-02
CUI: C1708957
Disease: Mediastinal Paraganglioma
Mediastinal Paraganglioma
5 0 2 6.1E-02 0 0
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III
5 0 2 6.1E-02 0 0
CUI: C2732413
Disease: Postexertional fatigue
Postexertional fatigue
5 0 2 6.1E-02 0 0
CUI: C3203503
Disease: Mixed delirium
Mixed delirium
5 0 2 6.1E-02 0 0
CUI: C0339084
Disease: Floppy lid syndrome
Floppy lid syndrome
6 0 2 5.9E-02 0 0
CUI: C0432593
Disease: Varus angulation
Varus angulation
6 0 2 5.9E-02 0 0
CUI: C1851720
Disease: Adrenocortical cytomegaly
Adrenocortical cytomegaly
6 0 2 5.9E-02 0 0
CUI: C1851722
Disease: Overgrowth of external genitalia
Overgrowth of external genitalia
6 0 2 5.9E-02 0 0
CUI: C1851733
Disease: Pancreatic hyperplasia
Pancreatic hyperplasia
6 0 2 5.9E-02 0 0
cutaneous squamous cell carcinoma of the head and neck
6 0 2 5.9E-02 0 0