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: C1853205
Disease: Glycosylphosphatidylinositol deficiency
Glycosylphosphatidylinositol deficiency 		5 0 2 0.12 0 0
CUI: C0151849
Disease: Alkaline phosphatase raised
Alkaline phosphatase raised 		55 0 7 0.11 0 0
CUI: C1827700
Disease: Luxation of lens
Luxation of lens 		7 0 2 0.11 0 0
CUI: C1842231
Disease: Broad metatarsal
Broad metatarsal 		7 0 2 0.11 0 0
CUI: C0263523
Disease: Micronychia (disorder)
Micronychia (disorder) 		60 0 7 0.11 0 0
CUI: C1314665
Disease: Serum alkaline phosphatase raised
Serum alkaline phosphatase raised 		67 0 7 9.6E-02 0 0
CUI: C0013581
Disease: Ectopia Lentis
Ectopia Lentis 		34 0 4 9.3E-02 0 0
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure 		73 0 7 8.9E-02 0 0
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly 		74 0 7 8.7E-02 0 0
CUI: C1842229
Disease: Broad metacarpals
Broad metacarpals 		12 0 2 8.7E-02 0 0
CUI: C0239479
Disease: Round face
Round face 		88 0 8 8.6E-02 0 0
CUI: C1857299
Disease: RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL
RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL 		13 0 2 8.3E-02 0 0
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion 		79 0 7 8.2E-02 0 0
CUI: C1833325
Disease: Thin bony cortex
Thin bony cortex 		14 0 2 8.0E-02 0 0
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