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: C0333205
Disease: Mural thrombus
Mural thrombus 		7 0 1 7.7E-02 0 0
CUI: C0425772
Disease: Premature development of the breasts
Premature development of the breasts 		7 0 1 7.7E-02 0 0
CUI: C0445118
Disease: Nephrotic range proteinuria
Nephrotic range proteinuria 		7 0 2 0.17 0 0
CUI: C1260883
Disease: Mural thrombus of heart
Mural thrombus of heart 		7 0 1 7.7E-02 0 0
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 2 0.17 0 0
CUI: C0268732
Disease: Nephritic syndrome
Nephritic syndrome 		8 0 1 7.1E-02 0 0
CUI: C0685837
Disease: Pure Gonadal Dysgenesis, 46, XX
Pure Gonadal Dysgenesis, 46, XX 		8 0 1 7.1E-02 0 0
CUI: C1567744
Disease: Alport Syndrome, Autosomal Recessive
Alport Syndrome, Autosomal Recessive 		8 0 1 7.1E-02 0 0
CUI: C3828492
Disease: Pre-Gestational Diabetes
Pre-Gestational Diabetes 		8 0 1 7.1E-02 0 0
CUI: C4024640
Disease: Aplasia/hypoplasia of the uterus
Aplasia/hypoplasia of the uterus 		8 0 1 7.1E-02 0 0
CUI: C4726566
Disease: Extracranial Solid Neoplasm
Extracranial Solid Neoplasm 		8 0 1 7.1E-02 0 0
CUI: C0426801
Disease: Broad clavicle
Broad clavicle 		9 0 1 6.7E-02 0 0
CUI: C0949595
Disease: Gonadal Dysgenesis, 46,XX
Gonadal Dysgenesis, 46,XX 		10 0 1 6.2E-02 0 0
CUI: C1849540
Disease: Delayed eruption of permanent teeth
Delayed eruption of permanent teeth 		10 0 1 6.2E-02 0 0
CUI: C4524264
Disease: Uncomplicated pyelonephritis
Uncomplicated pyelonephritis 		10 0 1 6.2E-02 0 0
CUI: C0241908
Disease: Hematuria, Benign Familial
Hematuria, Benign Familial 		11 0 1 5.9E-02 0 0
CUI: C0403399
Disease: Finnish congenital nephrotic syndrome
Finnish congenital nephrotic syndrome 		11 0 2 0.12 0 0
CUI: C0403440
Disease: Thin basement membrane disease
Thin basement membrane disease 		12 0 1 5.6E-02 0 0
CUI: C1842229
Disease: Broad metacarpals
Broad metacarpals 		12 0 1 5.6E-02 0 0
CUI: C4082168
Disease: Partial duplication of thumb phalanx
Partial duplication of thumb phalanx 		12 0 1 5.6E-02 0 0
CUI: C1567742
Disease: Alport Syndrome, X-Linked
Alport Syndrome, X-Linked 		13 0 1 5.3E-02 0 0
CUI: C4511620
Disease: Autosomal dominant tubulointerstitial kidney disease
Autosomal dominant tubulointerstitial kidney disease 		13 0 2 0.11 0 0
CUI: C4551680
Disease: Generalized osteoporosis
Generalized osteoporosis 		13 0 1 5.3E-02 0 0
CUI: C4021986
Disease: Hypoplasia of the ear cartilage
Hypoplasia of the ear cartilage 		14 0 2 0.11 0 0
CUI: C0220710
Disease: Medium-chain acyl-coenzyme A dehydrogenase deficiency
Medium-chain acyl-coenzyme A dehydrogenase deficiency 		15 0 1 4.8E-02 0 0