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: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent
11 0 1 2.8E-02 0 0
CUI: C0018552
Disease: Hamartoma
Hamartoma
4 0 1 3.4E-02 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
37 0 2 3.3E-02 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
31 0 2 3.6E-02 0 0
CUI: C0018923
Disease: Hemangiosarcoma
Hemangiosarcoma
2 0 1 3.7E-02 0 0
CUI: C0018932
Disease: Hematochezia
Hematochezia
2 0 1 3.7E-02 0 0
CUI: C0019322
Disease: Umbilical hernia
Umbilical hernia
17 0 1 2.4E-02 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
25 0 2 4.1E-02 0 0
CUI: C0020437
Disease: Hypercalcemia
Hypercalcemia
4 0 1 3.4E-02 0 0
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
25 0 1 2.0E-02 0 0
CUI: C0022821
Disease: Kyphosis deformity of spine
Kyphosis deformity of spine
9 0 1 2.9E-02 0 0
CUI: C0023418
Disease: leukemia
leukemia
2 0 1 3.7E-02 0 0
CUI: C0023462
Disease: Acute Megakaryocytic Leukemias
Acute Megakaryocytic Leukemias
4 0 2 7.1E-02 0 0
CUI: C0023798
Disease: Lipoma
Lipoma
5 0 1 3.3E-02 0 0
CUI: C0023882
Disease: Little's Disease
Little's Disease
6 0 1 3.2E-02 0 0
CUI: C0024221
Disease: Lymphangioma
Lymphangioma
1 0 1 3.8E-02 0 0
CUI: C0024421
Disease: Macroglossia
Macroglossia
2 0 1 3.7E-02 0 0
CUI: C0024433
Disease: Macrostomia
Macrostomia
10 0 1 2.9E-02 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism
46 0 2 2.9E-02 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
74 0 1 1.0E-02 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
162 0 3 1.6E-02 0 0
CUI: C0027092
Disease: Myopia
Myopia
45 0 2 2.9E-02 0 0
CUI: C0027960
Disease: Nevus
Nevus
4 0 2 7.1E-02 0 0
CUI: C0029128
Disease: Optic Disk Drusen
Optic Disk Drusen
3 0 1 3.6E-02 0 0
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy
18 0 1 2.3E-02 0 0