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: C0042781
Disease: Visceral Myopathy
Visceral Myopathy 		10 19 5 0.23 3 0.12
CUI: C0266200
Disease: Microcolon
Microcolon 		11 0 4 0.17 0 0
CUI: C0232475
Disease: Decreased peristalsis
Decreased peristalsis 		6 0 3 0.15 0 0
CUI: C0021847
Disease: Intestinal Pseudo-Obstruction
Intestinal Pseudo-Obstruction 		32 0 6 0.14 0 0
CUI: C0345244
Disease: Neuronal intestinal dysplasia
Neuronal intestinal dysplasia 		8 0 3 0.14 0 0
CUI: C1608393
Disease: Megacystis microcolon intestinal hypoperistalsis syndrome
Megacystis microcolon intestinal hypoperistalsis syndrome 		9 3 3 0.13 1 8.3E-02
CUI: C0266833
Disease: Visceral Myopathy, Familial
Visceral Myopathy, Familial 		2 1 2 0.12 1 1.0E-01
CUI: C1290162
Disease: Disorder of smooth muscle
Disorder of smooth muscle 		2 0 2 0.12 0 0
CUI: C1832589
Disease: Neuronal Intestinal Dysplasia, Type B
Neuronal Intestinal Dysplasia, Type B 		3 0 2 0.11 0 0
CUI: C1533174
Disease: Acute myeloid leukemia, inv(16)(p13q22)
Acute myeloid leukemia, inv(16)(p13q22) 		4 0 2 0.11 0 0
CUI: C0546275
Disease: Hypoganglionosis
Hypoganglionosis 		6 0 2 9.5E-02 0 0
CUI: C0334439
Disease: Malignant desmoplastic melanoma
Malignant desmoplastic melanoma 		7 0 2 9.1E-02 0 0
CUI: C1855311
Disease: Megacystis
Megacystis 		8 3 2 8.7E-02 2 0.18
CUI: C0037917
Disease: Spina Bifida Cystica
Spina Bifida Cystica 		21 0 3 8.6E-02 0 0
CUI: C0025160
Disease: Megacolon
Megacolon 		9 0 2 8.3E-02 0 0
CUI: C1848519
Disease: WAARDENBURG SYNDROME, TYPE 4A
WAARDENBURG SYNDROME, TYPE 4A 		12 0 2 7.4E-02 0 0
CUI: C0334507
Disease: Synovial sarcoma, biphasic
Synovial sarcoma, biphasic 		13 0 2 7.1E-02 0 0
CUI: C0878486
Disease: Arteriolosclerosis
Arteriolosclerosis 		13 0 2 7.1E-02 0 0
CUI: C0267809
Disease: Cirrhosis, Cryptogenic
Cirrhosis, Cryptogenic 		15 0 2 6.7E-02 0 0
CUI: C0345050
Disease: Congenital aneurysm of ascending aorta
Congenital aneurysm of ascending aorta 		16 0 2 6.5E-02 0 0
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		16 0 2 6.5E-02 0 0
CUI: C0018809
Disease: Heart Neoplasm
Heart Neoplasm 		17 0 2 6.2E-02 0 0
CUI: C0423318
Disease: Heterochromia iridis
Heterochromia iridis 		17 0 2 6.2E-02 0 0
CUI: C4042906
Disease: Mammary Analogue Secretory Carcinoma
Mammary Analogue Secretory Carcinoma 		17 0 2 6.2E-02 0 0
CUI: C0268393
Disease: Familial Cerebral Amyloid Angiopathy
Familial Cerebral Amyloid Angiopathy 		18 0 2 6.1E-02 0 0