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: C0020490
Disease: Hyperopia
Hyperopia
16 0 1 1.7E-02 0 0
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes
9 0 1 2.0E-02 0 0
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome
2 0 1 2.3E-02 0 0
CUI: C0023211
Disease: Left Bundle-Branch Block
Left Bundle-Branch Block
1 0 1 2.3E-02 0 0
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy
2 0 1 2.3E-02 0 0
CUI: C0023798
Disease: Lipoma
Lipoma
5 0 1 2.1E-02 0 0
CUI: C0024003
Disease: Lordosis
Lordosis
9 0 1 2.0E-02 0 0
CUI: C0024312
Disease: Lymphopenia
Lymphopenia
5 0 1 2.1E-02 0 0
CUI: C0025202
Disease: melanoma
melanoma
25 0 1 1.5E-02 0 0
CUI: C0026266
Disease: Mitral Valve Insufficiency
Mitral Valve Insufficiency
7 0 1 2.0E-02 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
336 0 7 1.9E-02 0 0
CUI: C0026848
Disease: Myopathy
Myopathy
37 0 5 6.7E-02 0 0
CUI: C0027092
Disease: Myopia
Myopia
45 0 2 2.3E-02 0 0
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome
12 0 1 1.9E-02 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
62 0 1 9.6E-03 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy
19 0 1 1.6E-02 0 0
Paroxysmal supraventricular tachycardia
1 0 1 2.3E-02 0 0
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy
18 0 1 1.7E-02 0 0
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome
5 0 1 2.1E-02 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
63 0 2 1.9E-02 0 0
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome
1 0 1 2.3E-02 0 0
CUI: C0037763
Disease: Spasm
Spasm
7 0 1 2.0E-02 0 0
CUI: C0038379
Disease: Strabismus
Strabismus
61 0 1 9.7E-03 0 0
CUI: C0039231
Disease: Tachycardia
Tachycardia
7 0 1 2.0E-02 0 0
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
18 0 1 1.7E-02 0 0