Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5
1 0 1 1.00 0 0
Malignant hyperthermia susceptibility type 5
1 0 1 1.00 0 0
Periodic paralysis with transient compartment-like syndrome
1 0 1 1.00 0 0
CUI: C0268445
Disease: Normokalemic Periodic Paralysis
Normokalemic Periodic Paralysis
2 0 1 0.50 0 0
CUI: C4025238
Disease: Generalized morning stiffness
Generalized morning stiffness
2 0 1 0.50 0 0
CUI: C4073214
Disease: Abnormality of masseter muscle
Abnormality of masseter muscle
2 0 1 0.50 0 0
Cardiomyocyte mitochondrial proliferation
2 0 1 0.50 0 0
Thyrotoxicosis with toxic single thyroid nodule
3 0 1 0.33 0 0
High-output congestive heart failure
3 0 1 0.33 0 0
CUI: C1838647
Disease: RETINITIS PIGMENTOSA 12 (disorder)
RETINITIS PIGMENTOSA 12 (disorder)
3 0 1 0.33 0 0
CUI: C4023104
Disease: Intermittent painful muscle spasms
Intermittent painful muscle spasms
3 0 1 0.33 0 0
AV Block Second Degree by ECG Finding
4 0 1 0.25 0 0
CUI: C4024709
Disease: Transient hypophosphatemia
Transient hypophosphatemia
4 0 1 0.25 0 0
Tooth development and eruption disorder
5 0 1 0.20 0 0
Second degree atrioventricular block
5 0 1 0.20 0 0
Tooth Agenesis, Selective, With Orofacial Cleft
5 0 1 0.20 0 0
Hypodontia Oligodontia with Orofacial Cleft
5 0 1 0.20 0 0
CUI: C3807306
Disease: Acute rhabdomyolysis
Acute rhabdomyolysis
5 0 1 0.20 0 0
CUI: C4022754
Disease: Episodic hypokalemia
Episodic hypokalemia
5 0 1 0.20 0 0
Hyperkalemia, diminished renal excretion
6 0 1 0.17 0 0
CUI: C0520878
Disease: Shortened PR interval
Shortened PR interval
6 0 1 0.17 0 0
CUI: C4021526
Disease: Exercise-induced rhabdomyolysis
Exercise-induced rhabdomyolysis
6 0 1 0.17 0 0
CUI: C4025572
Disease: Episodic flaccid weakness
Episodic flaccid weakness
6 0 1 0.17 0 0
CUI: C4310638
Disease: TOOTH AGENESIS, SELECTIVE, 9
TOOTH AGENESIS, SELECTIVE, 9
6 0 1 0.17 0 0
CUI: C0154143
Disease: Toxic multinodular goiter
Toxic multinodular goiter
7 0 1 0.14 0 0