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: C1857699
Disease: Palate telangiectasia
Palate telangiectasia
2 0 1 0.12 0 0
CUI: C1861248
Disease: Fingerpad telangiectases
Fingerpad telangiectases
2 0 1 0.12 0 0
Gonadal dysgenesis with female appearance, male
2 0 1 0.12 0 0
CUI: C4025853
Disease: Nasal mucosa telangiectasia
Nasal mucosa telangiectasia
2 0 1 0.12 0 0
CUI: C4025878
Disease: Tongue telangiectasia
Tongue telangiectasia
2 0 1 0.12 0 0
CUI: C4703595
Disease: Increased proinsulin:insulin ratio
Increased proinsulin:insulin ratio
2 0 1 0.12 0 0
Diffuse mesangial sclerosis (disorder)
22 0 3 0.12 0 0
Right to left cardiovascular shunt (finding)
3 0 1 0.11 0 0
High-output congestive heart failure
3 0 1 0.11 0 0
Gastrointestinal arteriovenous malformation
3 0 1 0.11 0 0
CUI: C1305904
Disease: Familial hematuria
Familial hematuria
23 0 3 0.11 0 0
CUI: C1562503
Disease: Vein of Galen Malformations
Vein of Galen Malformations
3 0 1 0.11 0 0
CUI: C1832940
Disease: JUVENILE POLYPOSIS OF STOMACH
JUVENILE POLYPOSIS OF STOMACH
3 0 1 0.11 0 0
CUI: C2931803
Disease: Deletion 11p13
Deletion 11p13
3 0 1 0.11 0 0
Autosomal dominant tubulointerstitial kidney disease
13 0 2 0.11 0 0
CUI: C0023439
Disease: Leukemia, Eosinophilic, Acute
Leukemia, Eosinophilic, Acute
4 0 1 1.0E-01 0 0
CUI: C0236801
Disease: Phobia, Specific
Phobia, Specific
4 0 1 1.0E-01 0 0
Congenital pulmonary arteriovenous malformation
4 0 1 1.0E-01 0 0
CUI: C0344542
Disease: Aniridia type 1
Aniridia type 1
4 0 1 1.0E-01 0 0
CUI: C0854242
Disease: Gastrointestinal angiodysplasia
Gastrointestinal angiodysplasia
4 0 1 1.0E-01 0 0
CUI: C1333003
Disease: Childhood Kidney Neoplasm
Childhood Kidney Neoplasm
4 0 1 1.0E-01 0 0
Dysfunction of lateral corticospinal tracts
4 0 1 1.0E-01 0 0
Elevated amniotic fluid alpha-fetoprotein
4 0 1 1.0E-01 0 0
CUI: C1853124
Disease: NEPHROTIC SYNDROME, TYPE 3
NEPHROTIC SYNDROME, TYPE 3
4 0 1 1.0E-01 0 0
Pulmonary arteriovenous malformation
4 0 1 1.0E-01 0 0