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: C0268312
Disease: Progressive intrahepatic cholestasis (disorder)
Progressive intrahepatic cholestasis (disorder) 		31 0 16 0.22 0 0
CUI: C4551898
Disease: Cholestasis, progressive familial intrahepatic 1
Cholestasis, progressive familial intrahepatic 1 		38 0 16 0.20 0 0
CUI: C0149841
Disease: Benign recurrent intrahepatic cholestasis
Benign recurrent intrahepatic cholestasis 		10 0 10 0.17 0 0
CUI: C1112213
Disease: Cholestasis in newborn
Cholestasis in newborn 		19 0 10 0.15 0 0
CUI: C4551984
Disease: Arthrogryposis with renal dysfunction and cholestasis syndrome
Arthrogryposis with renal dysfunction and cholestasis syndrome 		12 0 9 0.15 0 0
CUI: C0008372
Disease: Intrahepatic Cholestasis
Intrahepatic Cholestasis 		54 0 14 0.14 0 0
CUI: C3839589
Disease: Secondary osteoporosis
Secondary osteoporosis 		15 0 9 0.14 0 0
CUI: C1859722
Disease: Arthrogryposis, renal dysfunction, and cholestasis 1
Arthrogryposis, renal dysfunction, and cholestasis 1 		16 0 9 0.14 0 0
CUI: C1504525
Disease: Acute lymphoblastic leukemia recurrent
Acute lymphoblastic leukemia recurrent 		8 0 8 0.14 0 0
CUI: C4552224
Disease: B-cell aplasia
B-cell aplasia 		9 0 8 0.14 0 0
CUI: C0345288
Disease: Liver hyperplasia
Liver hyperplasia 		10 0 8 0.13 0 0
CUI: C0268287
Disease: Deficiency of steroid 21-monooxygenase
Deficiency of steroid 21-monooxygenase 		54 0 13 0.13 0 0
CUI: C4288302
Disease: Refractory Adult Acute Lymphoblastic Leukemia
Refractory Adult Acute Lymphoblastic Leukemia 		11 0 8 0.13 0 0
CUI: C0085280
Disease: Alagille Syndrome
Alagille Syndrome 		38 0 11 0.13 0 0
CUI: C0342345
Disease: Hypoparathyroidism - autosomal dominant
Hypoparathyroidism - autosomal dominant 		12 0 8 0.13 0 0
CUI: C0472813
Disease: X-linked agammaglobulinemia with growth hormone deficiency
X-linked agammaglobulinemia with growth hormone deficiency 		13 0 8 0.13 0 0
CUI: C0855082
Disease: Refractory Hodgkin Lymphoma
Refractory Hodgkin Lymphoma 		13 0 8 0.13 0 0
CUI: C4054085
Disease: Refractory Childhood Acute Lymphoblastic Leukemia
Refractory Childhood Acute Lymphoblastic Leukemia 		13 0 8 0.13 0 0
CUI: C1832615
Disease: HYPERPARATHYROIDISM, NEONATAL SEVERE
HYPERPARATHYROIDISM, NEONATAL SEVERE 		14 0 8 0.12 0 0
CUI: C3897729
Disease: Refractory Childhood Hodgkin Lymphoma
Refractory Childhood Hodgkin Lymphoma 		14 0 8 0.12 0 0
CUI: C4521228
Disease: Refractory Acute Lymphoblastic Leukemia
Refractory Acute Lymphoblastic Leukemia 		14 0 8 0.12 0 0
CUI: C0022353
Disease: Neonatal Jaundice
Neonatal Jaundice 		33 0 10 0.12 0 0
CUI: C0282609
Disease: Bone Marrow Neoplasms
Bone Marrow Neoplasms 		16 0 8 0.12 0 0
CUI: C0919976
Disease: Renal cancer metastatic
Renal cancer metastatic 		16 0 8 0.12 0 0
CUI: C1335723
Disease: Refractory Follicular Lymphoma
Refractory Follicular Lymphoma 		16 0 8 0.12 0 0