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: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder) 		9 0 8 0.73 0 0
CUI: C4021028
Disease: Pseudo-fractures
Pseudo-fractures 		10 0 8 0.67 0 0
CUI: C0268412
Disease: Infantile hypophosphatasia
Infantile hypophosphatasia 		12 0 8 0.57 0 0
CUI: C0205823
Disease: Pleomorphic Lipoma
Pleomorphic Lipoma 		13 0 8 0.53 0 0
CUI: C1848201
Disease: Subcortical Band Heterotopia
Subcortical Band Heterotopia 		30 0 10 0.33 0 0
CUI: C1842402
Disease: TROPICAL CALCIFIC PANCREATITIS
TROPICAL CALCIFIC PANCREATITIS 		24 0 8 0.31 0 0
CUI: C0020630
Disease: Hypophosphatasia
Hypophosphatasia 		27 0 8 0.28 0 0
CUI: C0432123
Disease: Sagittal craniosynostosis
Sagittal craniosynostosis 		35 0 8 0.22 0 0
CUI: C0151798
Disease: Hepatic necrosis
Hepatic necrosis 		44 0 9 0.20 0 0
CUI: C0265534
Disease: Scaphycephaly
Scaphycephaly 		43 0 8 0.18 0 0
CUI: C0342637
Disease: Hypocalciuric hypercalcemia, familial, type 1
Hypocalciuric hypercalcemia, familial, type 1 		46 0 8 0.17 0 0
CUI: C0520739
Disease: Hereditary pyropoikilocytosis
Hereditary pyropoikilocytosis 		47 0 8 0.16 0 0
CUI: C1370889
Disease: Liposarcoma, well differentiated
Liposarcoma, well differentiated 		54 0 8 0.14 0 0
CUI: C0276623
Disease: Chronic viral hepatitis
Chronic viral hepatitis 		59 0 8 0.13 0 0
CUI: C0342753
Disease: Glycogen storage disease due to acid maltase deficiency, late-onset
Glycogen storage disease due to acid maltase deficiency, late-onset 		8 0 2 0.12 0 0
CUI: C0234119
Disease: Neuromuscular inhibition
Neuromuscular inhibition 		72 0 8 0.11 0 0
CUI: C0451641
Disease: Urolithiasis
Urolithiasis 		72 0 8 0.11 0 0
CUI: C0339510
Disease: Vitelliform Macular Dystrophy
Vitelliform Macular Dystrophy 		74 0 8 0.11 0 0
CUI: C2347126
Disease: Microscopic Polyarteritis
Microscopic Polyarteritis 		77 0 8 0.10 0 0
CUI: C0349711
Disease: Sialic storage disease
Sialic storage disease 		1 0 1 1.0E-01 0 0
CUI: C0431379
Disease: Laminar heterotopia
Laminar heterotopia 		1 0 1 1.0E-01 0 0
CUI: C0849668
Disease: peri-menopausal
peri-menopausal 		1 0 1 1.0E-01 0 0
CUI: C1848070
Disease: Lissencephaly and agenesis of corpus callosum
Lissencephaly and agenesis of corpus callosum 		1 0 1 1.0E-01 0 0
CUI: C1963905
Disease: Infantile free sialic acid storage disease
Infantile free sialic acid storage disease 		1 0 1 1.0E-01 0 0
CUI: C2880120
Disease: Echovirus enteritis
Echovirus enteritis 		1 0 1 1.0E-01 0 0