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: C4024709
Disease: Transient hypophosphatemia
Transient hypophosphatemia
4 0 1 7.1E-02 0 0
Tooth development and eruption disorder
5 0 1 6.7E-02 0 0
Second degree atrioventricular block
5 0 1 6.7E-02 0 0
CUI: C0348616
Disease: Other restrictive cardiomyopathy
Other restrictive cardiomyopathy
5 0 1 6.7E-02 0 0
Tooth Agenesis, Selective, With Orofacial Cleft
5 0 1 6.7E-02 0 0
Hypodontia Oligodontia with Orofacial Cleft
5 0 1 6.7E-02 0 0
CUI: C3807306
Disease: Acute rhabdomyolysis
Acute rhabdomyolysis
5 0 1 6.7E-02 0 0
CUI: C4022754
Disease: Episodic hypokalemia
Episodic hypokalemia
5 0 1 6.7E-02 0 0
Hyperkalemia, diminished renal excretion
6 0 1 6.2E-02 0 0
CUI: C0520878
Disease: Shortened PR interval
Shortened PR interval
6 0 1 6.2E-02 0 0
CUI: C1739388
Disease: Birch pollen allergy
Birch pollen allergy
6 0 1 6.2E-02 0 0
CUI: C4021526
Disease: Exercise-induced rhabdomyolysis
Exercise-induced rhabdomyolysis
6 0 1 6.2E-02 0 0
CUI: C4025572
Disease: Episodic flaccid weakness
Episodic flaccid weakness
6 0 1 6.2E-02 0 0
CUI: C4310638
Disease: TOOTH AGENESIS, SELECTIVE, 9
TOOTH AGENESIS, SELECTIVE, 9
6 0 1 6.2E-02 0 0
CUI: C0154143
Disease: Toxic multinodular goiter
Toxic multinodular goiter
7 0 1 5.9E-02 0 0
Obstructive asymmetric septal hypertrophy
7 0 1 5.9E-02 0 0
Idiopathic hypertrophic subaortic stenosis
7 0 1 5.9E-02 0 0
Elevated creatine kinase after exercise
7 0 1 5.9E-02 0 0
CUI: C4025578
Disease: Late-onset proximal muscle weakness
Late-onset proximal muscle weakness
7 0 1 5.9E-02 0 0
CUI: C0004099
Disease: Asthma, Exercise-Induced
Asthma, Exercise-Induced
8 0 1 5.6E-02 0 0
CUI: C4024608
Disease: Necrotizing myopathy
Necrotizing myopathy
8 0 1 5.6E-02 0 0
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
9 0 1 5.3E-02 0 0
CUI: C3839736
Disease: Sensitization (disorder)
Sensitization (disorder)
9 0 1 5.3E-02 0 0
CUI: C4021553
Disease: Periodic hypokalemic paresis
Periodic hypokalemic paresis
9 0 1 5.3E-02 0 0
CUI: C3489529
Disease: Tooth Agenesis, Familial
Tooth Agenesis, Familial
10 0 1 5.0E-02 0 0