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: C1709780
Disease: Pyloric Gland Adenoma
Pyloric Gland Adenoma 		2 0 2 0.50 0 0
CUI: C1708747
Disease: Low grade appendiceal mucinous neoplasm
Low grade appendiceal mucinous neoplasm 		5 0 2 0.29 0 0
CUI: C0016064
Disease: Fibrous Dysplasia, Monostotic
Fibrous Dysplasia, Monostotic 		1 0 1 0.25 0 0
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms 		1 0 1 0.25 0 0
CUI: C0155747
Disease: Aneurysm of splenic artery
Aneurysm of splenic artery 		1 0 1 0.25 0 0
CUI: C0265593
Disease: Brachymetacarpia
Brachymetacarpia 		1 0 1 0.25 0 0
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 0.25 0 0
CUI: C0281952
Disease: Pseudohypothyroidism
Pseudohypothyroidism 		1 0 1 0.25 0 0
CUI: C0549608
Disease: VEINS/LYMPHATICS
VEINS/LYMPHATICS 		1 0 1 0.25 0 0
CUI: C1306574
Disease: Botryoid rhabdomyosarcoma
Botryoid rhabdomyosarcoma 		1 0 1 0.25 0 0
CUI: C1333081
Disease: Colloid Carcinoma of the Pancreas
Colloid Carcinoma of the Pancreas 		1 0 1 0.25 0 0
CUI: C1333308
Disease: Distal Bile Duct Carcinoma
Distal Bile Duct Carcinoma 		1 0 1 0.25 0 0
CUI: C1704453
Disease: Oncocytic Schneiderian papilloma
Oncocytic Schneiderian papilloma 		1 0 1 0.25 0 0
CUI: C1707332
Disease: Cellular Myxoma
Cellular Myxoma 		1 0 1 0.25 0 0
CUI: C1832443
Disease: Martinez-Frias Syndrome
Martinez-Frias Syndrome 		1 0 1 0.25 0 0
CUI: C1838329
Disease: APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS
APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS 		1 0 1 0.25 0 0
CUI: C1842881
Disease: Dilated aortic root
Dilated aortic root 		1 0 1 0.25 0 0
CUI: C2675383
Disease: POLYOSTOTIC FIBROUS DYSPLASIA, SOMATIC, MOSAIC
POLYOSTOTIC FIBROUS DYSPLASIA, SOMATIC, MOSAIC 		1 0 1 0.25 0 0
CUI: C2721606
Disease: Bladder dysplasia
Bladder dysplasia 		1 0 1 0.25 0 0
CUI: C2748662
Disease: Mitchell-Riley Syndrome
Mitchell-Riley Syndrome 		1 0 1 0.25 0 0
CUI: C3809005
Disease: CARDIOFACIOCUTANEOUS SYNDROME 2
CARDIOFACIOCUTANEOUS SYNDROME 2 		1 0 1 0.25 0 0
CUI: C4016140
Disease: PSEUDOHYPOPARATHYROIDISM, TYPE IA, WITH TESTOTOXICOSIS
PSEUDOHYPOPARATHYROIDISM, TYPE IA, WITH TESTOTOXICOSIS 		1 0 1 0.25 0 0
CUI: C4016403
Disease: BLADDER CANCER, TRANSITIONAL CELL, SOMATIC
BLADDER CANCER, TRANSITIONAL CELL, SOMATIC 		1 0 1 0.25 0 0
CUI: C4016796
Disease: COLORECTAL CANCER WITH CHROMOSOMAL INSTABILITY
COLORECTAL CANCER WITH CHROMOSOMAL INSTABILITY 		1 0 1 0.25 0 0
CUI: C4024097
Disease: Broad 1st metacarpal
Broad 1st metacarpal 		1 0 1 0.25 0 0