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: C0152190
Disease: Refractive amblyopia
Refractive amblyopia
1 0 1 0.33 0 0
Congenital stenosis of pulmonary valve
1 0 1 0.33 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT
1 0 1 0.33 0 0
CUI: C0265809
Disease: Double outlet left ventricle
Double outlet left ventricle
1 0 1 0.33 0 0
Congenital insufficiency of pulmonary valve
1 0 1 0.33 0 0
CUI: C0345140
Disease: Totally absent pericardium
Totally absent pericardium
1 0 1 0.33 0 0
Multiple Lentigines/LEOPARD syndrome
1 0 1 0.33 0 0
Increased subcutaneous truncal adipose tissue
1 0 1 0.33 0 0
CUI: C1861693
Disease: Cervical Vertebral Dysplasia
Cervical Vertebral Dysplasia
1 0 1 0.33 0 0
CUI: C2931296
Disease: Yorifuji Okuno syndrome
Yorifuji Okuno syndrome
1 0 1 0.33 0 0
CUI: C3280939
Disease: ATRIOVENTRICULAR SEPTAL DEFECT 5
ATRIOVENTRICULAR SEPTAL DEFECT 5
1 0 1 0.33 0 0
CUI: C3280943
Disease: ATRIAL SEPTAL DEFECT 9
ATRIAL SEPTAL DEFECT 9
1 0 1 0.33 0 0
Leukodystrophy, Dysmyelinating, with Oligodontia
1 0 1 0.33 0 0
PANCREATIC AGENESIS AND CONGENITAL HEART DEFECTS
1 0 1 0.33 0 0
HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES
1 10 1 0.33 1 8.3E-02
Congenital defect of the pericardium
1 0 1 0.33 0 0
Aplasia/Hypoplasia of the gallbladder
1 0 1 0.33 0 0
CUI: C4025162
Disease: Multiple digital exostoses
Multiple digital exostoses
1 0 1 0.33 0 0
CUI: C4025617
Disease: Atlantoaxial abnormality
Atlantoaxial abnormality
1 0 1 0.33 0 0
CUI: C4025818
Disease: Abnormality of skeletal maturation
Abnormality of skeletal maturation
1 0 1 0.33 0 0
Abnormality of the somatic nervous system
1 0 1 0.33 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease
2 0 1 0.25 0 0
Congenital hypoplasia of tricuspid valve
2 0 1 0.25 0 0
CUI: C0344772
Disease: Cleft leaflet of mitral valve
Cleft leaflet of mitral valve
2 0 1 0.25 0 0
CUI: C0391922
Disease: Hemorrhagic enteritis
Hemorrhagic enteritis
2 0 1 0.25 0 0