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: C0267581
Disease: Rectal Stenosis
Rectal Stenosis 		1 0 1 0.50 0 0
CUI: C0344923
Disease: Multiple ventricular septal defects
Multiple ventricular septal defects 		1 0 1 0.50 0 0
CUI: C4016468
Disease: VACTERL ASSOCIATION, X-LINKED
VACTERL ASSOCIATION, X-LINKED 		1 0 1 0.50 0 0
CUI: C4022693
Disease: Posteriorly placed anus
Posteriorly placed anus 		1 0 1 0.50 0 0
CUI: C4553656
Disease: Rectal Stenosis, CTCAE
Rectal Stenosis, CTCAE 		1 0 1 0.50 0 0
CUI: C1866091
Disease: Left-Right Axis Malformations
Left-Right Axis Malformations 		2 0 1 0.33 0 0
CUI: C2931228
Disease: VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS
VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS 		2 0 1 0.33 0 0
CUI: C0451840
Disease: Erosive osteoarthrosis
Erosive osteoarthrosis 		3 0 1 0.25 0 0
CUI: C1167664
Disease: Situs ambiguous
Situs ambiguous 		9 0 2 0.22 0 0
CUI: C0221215
Disease: Common atrioventricular canal
Common atrioventricular canal 		4 0 1 0.20 0 0
CUI: C1848599
Disease: VACTERL Association With Hydrocephalus
VACTERL Association With Hydrocephalus 		5 0 1 0.17 0 0
CUI: C1845026
Disease: Neural tube defects X-linked
Neural tube defects X-linked 		6 0 1 0.14 0 0
CUI: C0344760
Disease: Congenital atresia of mitral valve
Congenital atresia of mitral valve 		8 0 1 0.11 0 0
CUI: C4225671
Disease: VATER/VACTERL ASSOCIATION
VATER/VACTERL ASSOCIATION 		8 0 1 0.11 0 0
CUI: C4554010
Disease: Isomerism (body)
Isomerism (body) 		9 0 1 1.0E-01 0 0
CUI: C0242855
Disease: Congenital atresia of pulmonary valve
Congenital atresia of pulmonary valve 		11 0 1 8.3E-02 0 0
CUI: C0392482
Disease: Common atrium
Common atrium 		11 0 1 8.3E-02 0 0
CUI: C0011813
Disease: Dextrocardia
Dextrocardia 		30 0 2 6.7E-02 0 0
CUI: C0344490
Disease: Sacral agenesis
Sacral agenesis 		15 0 1 6.2E-02 0 0
CUI: C1735591
Disease: VACTERL Association
VACTERL Association 		15 0 1 6.2E-02 0 0
CUI: C1856659
Disease: Polysplenia
Polysplenia 		15 0 1 6.2E-02 0 0
CUI: C0021845
Disease: Intestinal Perforation
Intestinal Perforation 		16 0 1 5.9E-02 0 0
CUI: C0431363
Disease: Alobar Holoprosencephaly
Alobar Holoprosencephaly 		16 0 1 5.9E-02 0 0
CUI: C1840238
Disease: Midnasal stenosis
Midnasal stenosis 		16 0 1 5.9E-02 0 0
CUI: C4018871
Disease: Abnormality of the respiratory system
Abnormality of the respiratory system 		16 0 1 5.9E-02 0 0