Source: ALL
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: C1969404
Disease: Prominent frontal sinuses
Prominent frontal sinuses 		1 0 1 1.00 0 0
CUI: C1969410
Disease: Bidirectional ventricular ectopy
Bidirectional ventricular ectopy 		1 0 1 1.00 0 0
CUI: C1841648
Disease: Short mandibular rami
Short mandibular rami 		2 0 1 0.50 0 0
CUI: C2750061
Disease: Hypokalemic Periodic Paralysis, Type 2
Hypokalemic Periodic Paralysis, Type 2 		2 0 1 0.50 0 0
CUI: C2930902
Disease: Bidirectional tachycardia
Bidirectional tachycardia 		2 0 1 0.50 0 0
CUI: C1844509
Disease: Antegonial notching of mandible
Antegonial notching of mandible 		3 0 1 0.33 0 0
CUI: C1865018
Disease: Short QT Syndrome 3
Short QT Syndrome 3 		3 9 1 0.33 1 1.0E-01
CUI: C1865019
Disease: SHORT QT SYNDROME 2 (disorder)
SHORT QT SYNDROME 2 (disorder) 		3 0 1 0.33 0 0
CUI: C1969408
Disease: Prominent U wave
Prominent U wave 		3 0 1 0.33 0 0
CUI: C1865020
Disease: Short QT Syndrome 1
Short QT Syndrome 1 		4 0 1 0.25 0 0
CUI: C4021553
Disease: Periodic hypokalemic paresis
Periodic hypokalemic paresis 		9 0 1 0.11 0 0
CUI: C1849540
Disease: Delayed eruption of permanent teeth
Delayed eruption of permanent teeth 		10 0 1 1.0E-01 0 0
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome 		10 0 1 1.0E-01 0 0
CUI: C0344432
Disease: Ventricular tachycardia, polymorphic
Ventricular tachycardia, polymorphic 		11 11 1 9.1E-02 1 8.3E-02
CUI: C0266050
Disease: Failure of exfoliation of primary tooth
Failure of exfoliation of primary tooth 		12 0 1 8.3E-02 0 0
CUI: C3714580
Disease: Hypokalemic periodic paralysis type 1
Hypokalemic periodic paralysis type 1 		12 0 1 8.3E-02 0 0
CUI: C0151879
Disease: Shortened QT interval
Shortened QT interval 		13 0 1 7.7E-02 0 0
CUI: C4025741
Disease: Clinodactyly of the 5th toe
Clinodactyly of the 5th toe 		13 0 1 7.7E-02 0 0
CUI: C0268446
Disease: Thyrotoxic periodic paralysis
Thyrotoxic periodic paralysis 		15 0 1 6.7E-02 0 0
CUI: C1839730
Disease: Prieto X-linked mental retardation syndrome
Prieto X-linked mental retardation syndrome 		16 0 1 6.2E-02 0 0
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		18 10 1 5.6E-02 1 9.1E-02
CUI: C1279412
Disease: periodic paralysis (finding)
periodic paralysis (finding) 		18 11 1 5.6E-02 1 8.3E-02
CUI: C0238358
Disease: Hypokalemic periodic paralysis
Hypokalemic periodic paralysis 		19 0 1 5.3E-02 0 0
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		22 0 1 4.5E-02 0 0
CUI: C1563715
Disease: Andersen Syndrome
Andersen Syndrome 		23 38 1 4.3E-02 1 2.6E-02