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: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 7.7E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 7.7E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 7.7E-02 0 0
CUI: C0423431
Disease: Subretinal exudate
Subretinal exudate 		1 0 1 7.7E-02 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 7.7E-02 0 0
CUI: C0852085
Disease: Congenital connective tissue disorder
Congenital connective tissue disorder 		1 0 1 7.7E-02 0 0
CUI: C1112654
Disease: Peripheral artery dissection
Peripheral artery dissection 		1 0 1 7.7E-02 0 0
CUI: C1835130
Disease: Premature calcification of mitral annulus
Premature calcification of mitral annulus 		1 0 1 7.7E-02 0 0
CUI: C1844579
Disease: Exudative Vitreoretinopathy, Familial, X-Linked Recessive
Exudative Vitreoretinopathy, Familial, X-Linked Recessive 		1 0 1 7.7E-02 0 0
CUI: C1848392
Disease: Zunich neuroectodermal syndrome
Zunich neuroectodermal syndrome 		1 0 1 7.7E-02 0 0
CUI: C1861456
Disease: Stiff Skin Syndrome
Stiff Skin Syndrome 		1 0 1 7.7E-02 0 0
CUI: C2748355
Disease: Descending thoracic aortic dissection
Descending thoracic aortic dissection 		1 0 1 7.7E-02 0 0
CUI: C2751316
Disease: Glaucoma 3, Primary Congenital, D
Glaucoma 3, Primary Congenital, D 		1 0 1 7.7E-02 0 0
CUI: C2931588
Disease: GEMSS syndrome
GEMSS syndrome 		1 0 1 7.7E-02 0 0
CUI: C3280054
Disease: GELEOPHYSIC DYSPLASIA 2
GELEOPHYSIC DYSPLASIA 2 		1 0 1 7.7E-02 0 0
CUI: C3280153
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 17
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 17 		1 0 1 7.7E-02 0 0
CUI: C3280203
Disease: WARBURG MICRO SYNDROME 3
WARBURG MICRO SYNDROME 3 		1 0 1 7.7E-02 0 0
CUI: C3538951
Disease: MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA
MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA 		1 0 1 7.7E-02 0 0
CUI: C3541518
Disease: ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT
ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT 		1 0 1 7.7E-02 0 0
CUI: C3553637
Disease: HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 		1 0 1 7.7E-02 0 0
CUI: C3553785
Disease: WEILL-MARCHESANI SYNDROME 3
WEILL-MARCHESANI SYNDROME 3 		1 0 1 7.7E-02 0 0
CUI: C3805726
Disease: Medial rotation of the medial malleolus
Medial rotation of the medial malleolus 		1 0 1 7.7E-02 0 0
CUI: C3810354
Disease: HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4 		1 0 1 7.7E-02 0 0
CUI: C4016052
Disease: MARFAN SYNDROME, SEVERE CLASSIC
MARFAN SYNDROME, SEVERE CLASSIC 		1 0 1 7.7E-02 0 0
CUI: C4016053
Disease: MARFAN SYNDROME, MILD VARIABLE
MARFAN SYNDROME, MILD VARIABLE 		1 0 1 7.7E-02 0 0