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: C0022575
Disease: Keratoconjunctivitis Sicca
Keratoconjunctivitis Sicca
4 3 1 2.2E-02 1 2.2E-03
CUI: C0023211
Disease: Left Bundle-Branch Block
Left Bundle-Branch Block
1 0 1 2.3E-02 0 0
CUI: C0023380
Disease: Lethargy
Lethargy
5 5 1 2.1E-02 1 2.2E-03
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: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
20 21 1 1.6E-02 1 2.2E-03
CUI: C0027960
Disease: Nevus
Nevus
4 7 1 2.2E-02 1 2.2E-03
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: C0033300
Disease: Progeria
Progeria
1 20 1 2.3E-02 2 4.3E-03
CUI: C0035410
Disease: Rhabdomyolysis
Rhabdomyolysis
13 14 1 1.8E-02 1 2.2E-03
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome
5 0 1 2.1E-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: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
2 5 1 2.3E-02 1 2.2E-03
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