Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Congenital hernia of foramen of Morgagni
19 0 19 0.90 0 0
CUI: C2677362
Disease: Alveolar capillary dysplasia
Alveolar capillary dysplasia
7 0 3 0.12 0 0
CUI: C0333244
Disease: Transient edema
Transient edema
2 0 2 9.5E-02 0 0
CUI: C0235833
Disease: Congenital diaphragmatic hernia
Congenital diaphragmatic hernia
239 0 21 8.8E-02 0 0
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced
5 0 2 8.3E-02 0 0
CUI: C0242404
Disease: Myofibroblastoma
Myofibroblastoma
6 0 2 8.0E-02 0 0
CUI: C0553980
Disease: Endomyocardial Fibrosis
Endomyocardial Fibrosis
20 0 3 7.9E-02 0 0
CUI: C0392400
Disease: Diffuse malignant mesothelioma
Diffuse malignant mesothelioma
7 0 2 7.7E-02 0 0
Chronic myeloid leukemia, BCR/ABL-positive
7 0 2 7.7E-02 0 0
CUI: C0741237
Disease: arthritis symptoms
arthritis symptoms
9 0 2 7.1E-02 0 0
CUI: C0024214
Disease: Lymphangiectasis
Lymphangiectasis
11 0 2 6.7E-02 0 0
Congenital atresia of pulmonary valve
11 0 2 6.7E-02 0 0
CUI: C0281508
Disease: Desmoplastic Small Round Cell Tumor
Desmoplastic Small Round Cell Tumor
43 0 4 6.7E-02 0 0
CUI: C1518716
Disease: Ovarian gonadoblastoma
Ovarian gonadoblastoma
11 0 2 6.7E-02 0 0
CUI: C4025892
Disease: Abnormality of the labia
Abnormality of the labia
11 0 2 6.7E-02 0 0
CUI: C4510744
Disease: 46,XY partial gonadal dysgenesis
46,XY partial gonadal dysgenesis
11 0 2 6.7E-02 0 0
CUI: C1515283
Disease: Testicular gonadoblastoma
Testicular gonadoblastoma
12 0 2 6.5E-02 0 0
CUI: C2676137
Disease: Diamond-Blackfan Anemia 1
Diamond-Blackfan Anemia 1
12 0 2 6.5E-02 0 0
CUI: C3888044
Disease: Nephrogenic Systemic Fibrosis
Nephrogenic Systemic Fibrosis
12 0 2 6.5E-02 0 0
CUI: C0033054
Disease: Prenatal Exposure Delayed Effects
Prenatal Exposure Delayed Effects
13 0 2 6.2E-02 0 0
CUI: C0154823
Disease: Retinal defect
Retinal defect
13 0 2 6.2E-02 0 0
CUI: C0302885
Disease: Testicular dysgenesis
Testicular dysgenesis
13 0 2 6.2E-02 0 0
CUI: C3495489
Disease: Rieger eye malformation sequence
Rieger eye malformation sequence
13 0 2 6.2E-02 0 0
CUI: C4025895
Disease: Abnormality of the scrotum
Abnormality of the scrotum
13 0 2 6.2E-02 0 0
CUI: C4285959
Disease: Erosive arthritis
Erosive arthritis
13 0 2 6.2E-02 0 0