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: C0027651
Disease: Neoplasms
Neoplasms
10161 0 8 7.9E-04 0 0
Sensorineural Hearing Loss (disorder)
783 0 7 8.9E-03 0 0
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
6941 0 6 8.6E-04 0 0
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
8621 0 6 7.0E-04 0 0
CUI: C0025322
Disease: Premature Menopause
Premature Menopause
299 0 6 2.0E-02 0 0
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea
129 0 6 4.4E-02 0 0
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
6776 0 6 8.8E-04 0 0
CUI: C1384666
Disease: hearing impairment
hearing impairment
740 0 6 8.0E-03 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 5 5.7E-03 0 0
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
333 0 5 1.5E-02 0 0
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
2542 0 5 2.0E-03 0 0
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
2563 0 5 1.9E-03 0 0
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
6626 0 5 7.5E-04 0 0
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
8221 0 5 6.1E-04 0 0
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
2165 0 5 2.3E-03 0 0
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
2084 0 4 1.9E-03 0 0
CUI: C0026848
Disease: Myopathy
Myopathy
634 0 4 6.2E-03 0 0
CUI: C0036572
Disease: Seizures
Seizures
2152 0 4 1.9E-03 0 0
CUI: C0266399
Disease: Infantile uterus
Infantile uterus
43 0 4 7.5E-02 0 0
Conventional (Clear Cell) Renal Cell Carcinoma
2346 0 4 1.7E-03 0 0
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
4502 0 4 8.9E-04 0 0
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
6243 0 4 6.4E-04 0 0
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
5725 0 4 7.0E-04 0 0
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
2841 0 4 1.4E-03 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
1098 0 3 2.7E-03 0 0