Source: ALL
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: C0023441
Disease: Leukemia, Experimental
Leukemia, Experimental 		1 0 1 3.6E-02 0 0
CUI: C0085699
Disease: Cardiac cirrhosis
Cardiac cirrhosis 		1 0 1 3.6E-02 0 0
CUI: C0265809
Disease: Double outlet left ventricle
Double outlet left ventricle 		1 0 1 3.6E-02 0 0
CUI: C0265914
Disease: Anomalous pulmonary vein
Anomalous pulmonary vein 		1 0 1 3.6E-02 0 0
CUI: C0266336
Disease: Congenital absence of bladder
Congenital absence of bladder 		1 0 1 3.6E-02 0 0
CUI: C0268373
Disease: Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome 		1 0 1 3.6E-02 0 0
CUI: C0269852
Disease: Vasa Previa
Vasa Previa 		1 0 1 3.6E-02 0 0
CUI: C0334390
Disease: Acinar cell tumor
Acinar cell tumor 		1 0 1 3.6E-02 0 0
CUI: C0345140
Disease: Totally absent pericardium
Totally absent pericardium 		1 0 1 3.6E-02 0 0
CUI: C0348872
Disease: Disorders of both mitral and tricuspid valves
Disorders of both mitral and tricuspid valves 		1 1 1 3.6E-02 1 0.20
CUI: C0349539
Disease: Malignant melanoma of rectum
Malignant melanoma of rectum 		1 0 1 3.6E-02 0 0
CUI: C0392180
Disease: Necrosis of placenta
Necrosis of placenta 		1 0 1 3.6E-02 0 0
CUI: C0544862
Disease: Neurocutaneous melanosis
Neurocutaneous melanosis 		1 0 1 3.6E-02 0 0
CUI: C0595928
Disease: Serum calcium increased
Serum calcium increased 		1 0 1 3.6E-02 0 0
CUI: C0741918
Disease: Structural cardiac defects
Structural cardiac defects 		1 0 1 3.6E-02 0 0
CUI: C1167752
Disease: Graft ischaemia
Graft ischaemia 		1 0 1 3.6E-02 0 0
CUI: C1280777
Disease: displaced uterus
displaced uterus 		1 0 1 3.6E-02 0 0
CUI: C1321871
Disease: childhood acute myeloid leukemia/other myeloid malignancies
childhood acute myeloid leukemia/other myeloid malignancies 		1 0 1 3.6E-02 0 0
CUI: C1334691
Disease: Melanomatosis
Melanomatosis 		1 0 1 3.6E-02 0 0
CUI: C1335461
Disease: Postsurgical Stage I Hepatoblastoma
Postsurgical Stage I Hepatoblastoma 		1 0 1 3.6E-02 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 1 1 3.6E-02 1 0.20
CUI: C1832612
Disease: Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 		1 0 1 3.6E-02 0 0
CUI: C1845292
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP B
FANCONI ANEMIA, COMPLEMENTATION GROUP B 		1 0 1 3.6E-02 0 0
CUI: C1848392
Disease: Zunich neuroectodermal syndrome
Zunich neuroectodermal syndrome 		1 0 1 3.6E-02 0 0
CUI: C1848600
Disease: Vater Association With Hydrocephalus
Vater Association With Hydrocephalus 		1 0 1 3.6E-02 0 0