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: C1848200
Disease: SUBCORTICAL BAND HETEROTOPIA, X-LINKED
SUBCORTICAL BAND HETEROTOPIA, X-LINKED 		10 0 9 0.20 0 0
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder) 		9 0 8 0.18 0 0
CUI: C4021028
Disease: Pseudo-fractures
Pseudo-fractures 		10 0 8 0.17 0 0
CUI: C0268412
Disease: Infantile hypophosphatasia
Infantile hypophosphatasia 		12 0 8 0.17 0 0
CUI: C0205823
Disease: Pleomorphic Lipoma
Pleomorphic Lipoma 		13 0 8 0.16 0 0
CUI: C0276623
Disease: Chronic viral hepatitis
Chronic viral hepatitis 		59 0 14 0.16 0 0
CUI: C1848201
Disease: Subcortical Band Heterotopia
Subcortical Band Heterotopia 		30 0 9 0.14 0 0
CUI: C1842402
Disease: TROPICAL CALCIFIC PANCREATITIS
TROPICAL CALCIFIC PANCREATITIS 		24 0 8 0.13 0 0
CUI: C0020630
Disease: Hypophosphatasia
Hypophosphatasia 		27 0 8 0.13 0 0
CUI: C0432123
Disease: Sagittal craniosynostosis
Sagittal craniosynostosis 		35 0 8 0.11 0 0
CUI: C0265534
Disease: Scaphycephaly
Scaphycephaly 		43 0 8 0.10 0 0
CUI: C0342637
Disease: Hypocalciuric hypercalcemia, familial, type 1
Hypocalciuric hypercalcemia, familial, type 1 		46 0 8 9.8E-02 0 0
CUI: C0520739
Disease: Hereditary pyropoikilocytosis
Hereditary pyropoikilocytosis 		47 0 8 9.6E-02 0 0
CUI: C1963135
Disease: Hepatic Necrosis, CTCAE 3.0
Hepatic Necrosis, CTCAE 3.0 		4 0 4 9.1E-02 0 0
CUI: C4554166
Disease: Hepatic Necrosis, CTCAE 5.0
Hepatic Necrosis, CTCAE 5.0 		4 0 4 9.1E-02 0 0
CUI: C2347126
Disease: Microscopic Polyarteritis
Microscopic Polyarteritis 		77 0 10 9.0E-02 0 0
CUI: C1855038
Disease: Hepatocellular necrosis
Hepatocellular necrosis 		41 0 7 9.0E-02 0 0
CUI: C1370889
Disease: Liposarcoma, well differentiated
Liposarcoma, well differentiated 		54 0 8 8.9E-02 0 0
CUI: C0151846
Disease: Periosteal Disorder
Periosteal Disorder 		80 0 10 8.8E-02 0 0
CUI: C0041948
Disease: Uremia
Uremia 		110 0 12 8.5E-02 0 0
CUI: C0339510
Disease: Vitelliform Macular Dystrophy
Vitelliform Macular Dystrophy 		74 0 9 8.3E-02 0 0
CUI: C1698259
Disease: HCV coinfection
HCV coinfection 		37 0 6 8.0E-02 0 0
CUI: C0019202
Disease: Hepatolenticular Degeneration
Hepatolenticular Degeneration 		146 0 14 8.0E-02 0 0
CUI: C0221002
Disease: Hyperparathyroidism, Primary
Hyperparathyroidism, Primary 		115 0 11 7.4E-02 0 0
CUI: C0234119
Disease: Neuromuscular inhibition
Neuromuscular inhibition 		72 0 8 7.4E-02 0 0