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: C0002418
Disease: Amblyopia
Amblyopia
17 0 1 2.7E-02 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
9 0 1 3.4E-02 0 0
CUI: C0004096
Disease: Asthma
Asthma
18 0 1 2.6E-02 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
37 0 1 1.8E-02 0 0
CUI: C0006009
Disease: Borderline intellectual disability
Borderline intellectual disability
3 0 1 4.3E-02 0 0
CUI: C0006157
Disease: Breech Presentation
Breech Presentation
10 0 1 3.3E-02 0 0
CUI: C0006664
Disease: Calcinosis cutis
Calcinosis cutis
1 0 1 4.8E-02 0 0
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
15 0 1 2.9E-02 0 0
CUI: C0011981
Disease: Diaphragmatic Eventration
Diaphragmatic Eventration
6 0 1 3.8E-02 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
34 0 1 1.9E-02 0 0
CUI: C0014877
Disease: Esotropia
Esotropia
33 0 1 1.9E-02 0 0
CUI: C0017097
Disease: Gardner Syndrome
Gardner Syndrome
1 0 1 4.8E-02 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma
6 0 1 3.8E-02 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
37 0 2 3.6E-02 0 0
CUI: C0018923
Disease: Hemangiosarcoma
Hemangiosarcoma
2 0 1 4.5E-02 0 0
CUI: C0020502
Disease: Hyperparathyroidism
Hyperparathyroidism
1 0 1 4.8E-02 0 0
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
63 0 1 1.2E-02 0 0
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia
2 0 1 4.5E-02 0 0
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
25 0 1 2.2E-02 0 0
CUI: C0021846
Disease: Intestinal Polyps
Intestinal Polyps
1 0 1 4.8E-02 0 0
CUI: C0023462
Disease: Acute Megakaryocytic Leukemias
Acute Megakaryocytic Leukemias
4 0 1 4.2E-02 0 0
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
5 0 1 4.0E-02 0 0
CUI: C0023882
Disease: Little's Disease
Little's Disease
6 0 1 3.8E-02 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
28 0 1 2.1E-02 0 0
CUI: C0028754
Disease: Obesity
Obesity
24 0 1 2.3E-02 0 0