Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Weill-Marchesani Syndrome, Autosomal Recessive
3 0 3 1.00 0 0
CUI: C4552002
Disease: WEILL-MARCHESANI SYNDROME 1
WEILL-MARCHESANI SYNDROME 1
2 0 2 0.67 0 0
CUI: C0265313
Disease: Weill-Marchesani syndrome
Weill-Marchesani syndrome
5 0 3 0.60 0 0
CUI: C2750787
Disease: Weill-Marchesani-Like Syndrome
Weill-Marchesani-Like Syndrome
5 0 3 0.60 0 0
CUI: C0424693
Disease: Broad skull
Broad skull
3 0 2 0.50 0 0
CUI: C4021391
Disease: Broad phalanges of the hand
Broad phalanges of the hand
4 0 2 0.40 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm
1 0 1 0.33 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia
1 0 1 0.33 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome
1 0 1 0.33 0 0
Congenital dilatation of pulmonary artery
1 0 1 0.33 0 0
Congenital connective tissue disorder
1 0 1 0.33 0 0
CUI: C1112654
Disease: Peripheral artery dissection
Peripheral artery dissection
1 0 1 0.33 0 0
CUI: C1562061
Disease: Microspherophakia
Microspherophakia
9 0 3 0.33 0 0
Premature calcification of mitral annulus
1 0 1 0.33 0 0
CUI: C1851286
Disease: Ectopia lentis isolated
Ectopia lentis isolated
5 3 2 0.33 1 4.0E-02
CUI: C1861456
Disease: Stiff Skin Syndrome
Stiff Skin Syndrome
1 26 1 0.33 22 0.81
Descending thoracic aortic dissection
1 0 1 0.33 0 0
CUI: C2751316
Disease: Glaucoma 3, Primary Congenital, D
Glaucoma 3, Primary Congenital, D
1 0 1 0.33 0 0
CUI: C2931588
Disease: GEMSS syndrome
GEMSS syndrome
1 0 1 0.33 0 0
CUI: C3280054
Disease: GELEOPHYSIC DYSPLASIA 2
GELEOPHYSIC DYSPLASIA 2
1 27 1 0.33 22 0.79
MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA
1 0 1 0.33 0 0
ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT
1 24 1 0.33 22 0.88
CUI: C3553785
Disease: WEILL-MARCHESANI SYNDROME 3
WEILL-MARCHESANI SYNDROME 3
1 0 1 0.33 0 0
Medial rotation of the medial malleolus
1 0 1 0.33 0 0
CUI: C4016052
Disease: MARFAN SYNDROME, SEVERE CLASSIC
MARFAN SYNDROME, SEVERE CLASSIC
1 0 1 0.33 0 0