Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Malignant Testicular Germ Cell Tumor
128 62 107 0.39 10 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
5473 1962 160 2.9E-02 9 4.5E-03
Malignant neoplasm of urinary bladder
2113 316 107 4.7E-02 8 2.4E-02
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
1881 283 89 4.4E-02 7 2.3E-02
CUI: C0001080
Disease: Achondroplasia
Achondroplasia
46 21 2 6.7E-03 6 0.13
CUI: C0039590
Disease: Testicular Neoplasms
Testicular Neoplasms
124 31 34 9.9E-02 6 0.11
Lacrimoauriculodentodigital syndrome
5 33 1 3.9E-03 6 0.10
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
NEVUS, EPIDERMAL (disorder)
14 17 2 7.5E-03 6 0.14
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder)
16 42 1 3.7E-03 6 9.0E-02
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2
11 17 1 3.8E-03 6 0.14
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor
208 93 46 0.11 6 5.1E-02
CUI: C1864436
Disease: Muenke Syndrome
Muenke Syndrome
3 11 1 3.9E-03 6 0.17
CUI: C1864852
Disease: CATSHL syndrome
CATSHL syndrome
1 10 1 4.0E-03 6 0.17
THANATOPHORIC DYSPLASIA, TYPE I (disorder)
20 18 2 7.4E-03 6 0.14
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans
3 9 1 3.9E-03 6 0.18
CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder)
1 8 1 4.0E-03 6 0.18
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis
488 90 15 2.1E-02 5 4.3E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms
10161 1644 221 2.2E-02 5 3.0E-03
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
8621 1641 222 2.6E-02 4 2.4E-03
CUI: C0039743
Disease: Thanatophoric Dysplasia
Thanatophoric Dysplasia
12 10 2 7.6E-03 4 0.11
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
1597 326 88 5.0E-02 4 1.1E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
8221 1374 219 2.7E-02 4 2.9E-03
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
1075 276 62 4.9E-02 4 1.3E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
1708 1577 56 2.9E-02 4 2.5E-03
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
1098 73 43 3.3E-02 3 3.0E-02