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: C0000731
Disease: Abdomen distended
Abdomen distended
6 0 1 2.9E-02 0 0
CUI: C1852464
Disease: Abnormality of the cervical spine
Abnormality of the cervical spine
4 0 1 3.1E-02 0 0
CUI: C1848873
Disease: Abnormality of the diaphragm
Abnormality of the diaphragm
2 0 1 3.3E-02 0 0
CUI: C4021789
Disease: Abnormality of the vertebral column
Abnormality of the vertebral column
4 0 1 3.1E-02 0 0
CUI: C4317146
Disease: Acid reflux
Acid reflux
50 0 1 1.3E-02 0 0
CUI: C3553748
Disease: ADAMS-OLIVER SYNDROME 3
ADAMS-OLIVER SYNDROME 3
1 5 1 3.4E-02 1 1.6E-02
CUI: C4024790
Disease: Adult-onset night blindness
Adult-onset night blindness
2 0 1 3.3E-02 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly
9 0 1 2.7E-02 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
37 0 1 1.5E-02 0 0
CUI: C0431663
Disease: Bilateral Cryptorchidism
Bilateral Cryptorchidism
5 0 1 3.0E-02 0 0
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF
1 0 1 3.4E-02 0 0
CUI: C1849089
Disease: Broad forehead
Broad forehead
11 0 1 2.6E-02 0 0
CUI: C0232180
Disease: Cardiac shunt
Cardiac shunt
1 0 1 3.4E-02 0 0
CARDIOMYOPATHY WITH OR WITHOUT SKELETAL MYOPATHY
1 0 1 3.4E-02 0 0
CUI: C0086543
Disease: Cataract
Cataract
13 13 1 2.4E-02 1 1.4E-02
CUI: C3805412
Disease: CATARACT 41
CATARACT 41
1 0 1 3.4E-02 0 0
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia
20 0 1 2.1E-02 0 0
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
7 14 1 2.9E-02 1 1.4E-02
CUI: C1266042
Disease: Chromophobe Renal Cell Carcinoma
Chromophobe Renal Cell Carcinoma
3 0 2 6.7E-02 0 0
CUI: C1735903
Disease: Chronic acidosis
Chronic acidosis
1 0 1 3.4E-02 0 0
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
43 0 1 1.4E-02 0 0
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
31 0 1 1.7E-02 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy
16 0 1 2.3E-02 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies
20 0 1 2.1E-02 0 0
CUI: C3888018
Disease: Congenital Hyperinsulinism
Congenital Hyperinsulinism
2 10 2 6.9E-02 1 1.5E-02