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: C0406409
Disease: Aquagenic pruritus
Aquagenic pruritus
1 0 1 9.1E-02 0 0
CARDIOMYOPATHY, DILATED, 1D (disorder)
1 0 1 9.1E-02 0 0
Cardiomyopathy, Familial Hypertrophic, 2
1 0 1 9.1E-02 0 0
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5
1 0 1 9.1E-02 0 0
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
1 0 1 9.1E-02 0 0
THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1
1 0 1 9.1E-02 0 0
Malignant hyperthermia susceptibility type 5
1 0 1 9.1E-02 0 0
Modic type vertebral endplate changes
1 0 1 9.1E-02 0 0
Periodic paralysis with transient compartment-like syndrome
1 0 1 9.1E-02 0 0
CUI: C0268445
Disease: Normokalemic Periodic Paralysis
Normokalemic Periodic Paralysis
2 0 1 8.3E-02 0 0
CUI: C0278586
Disease: Metastatic Ewing's Sarcoma
Metastatic Ewing's Sarcoma
2 0 1 8.3E-02 0 0
Adult Glycogen Storage Disease Type II
2 0 1 8.3E-02 0 0
Glycogen Storage Disease Type II, Juvenile
2 0 1 8.3E-02 0 0
CUI: C1304191
Disease: Autoimmune urticaria
Autoimmune urticaria
2 0 1 8.3E-02 0 0
Progressive Familial Heart Block, Type II
2 0 1 8.3E-02 0 0
CUI: C4025238
Disease: Generalized morning stiffness
Generalized morning stiffness
2 0 1 8.3E-02 0 0
CUI: C4073214
Disease: Abnormality of masseter muscle
Abnormality of masseter muscle
2 0 1 8.3E-02 0 0
Cardiomyocyte mitochondrial proliferation
2 0 1 8.3E-02 0 0
CUI: C0015745
Disease: Feeding behaviors
Feeding behaviors
3 0 1 7.7E-02 0 0
Thyrotoxicosis with toxic single thyroid nodule
3 0 1 7.7E-02 0 0
High-output congestive heart failure
3 0 1 7.7E-02 0 0
CUI: C1838647
Disease: RETINITIS PIGMENTOSA 12 (disorder)
RETINITIS PIGMENTOSA 12 (disorder)
3 0 1 7.7E-02 0 0
CUI: C4023104
Disease: Intermittent painful muscle spasms
Intermittent painful muscle spasms
3 0 1 7.7E-02 0 0
Glycogen Storage Disease Type II, Infantile
4 0 1 7.1E-02 0 0
AV Block Second Degree by ECG Finding
4 0 1 7.1E-02 0 0