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: C1845667
Disease: RETINITIS PIGMENTOSA 3
RETINITIS PIGMENTOSA 3 		8 31 6 0.19 3 8.6E-02
CUI: C2681923
Disease: RETINITIS PIGMENTOSA 2 (disorder)
RETINITIS PIGMENTOSA 2 (disorder) 		9 6 6 0.19 1 8.3E-02
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 7 0.15 0 0
CUI: C0268505
Disease: Ocular albinism, type II
Ocular albinism, type II 		7 0 3 9.1E-02 0 0
CUI: C1859807
Disease: AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder) 		25 0 4 8.0E-02 0 0
CUI: C0268542
Disease: Ornithine carbamoyltransferase deficiency
Ornithine carbamoyltransferase deficiency 		17 0 3 7.0E-02 0 0
CUI: C0155360
Disease: Staphyloma posticum
Staphyloma posticum 		4 0 2 6.5E-02 0 0
CUI: C0340434
Disease: Dystrophic cardiomyopathy
Dystrophic cardiomyopathy 		5 0 2 6.2E-02 0 0
CUI: C1858593
Disease: Limb-girdle muscular dystrophy, type 2E
Limb-girdle muscular dystrophy, type 2E 		5 0 2 6.2E-02 0 0
CUI: C4048273
Disease: Chorioretinal atrophy
Chorioretinal atrophy 		24 0 3 6.0E-02 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 4 6.0E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome 		42 0 4 6.0E-02 0 0
CUI: C0018425
Disease: Gyrate Atrophy
Gyrate Atrophy 		8 0 2 5.7E-02 0 0
CUI: C1300585
Disease: Small cell carcinoma of prostate
Small cell carcinoma of prostate 		8 0 2 5.7E-02 0 0
CUI: C0265339
Disease: Borjeson-Forssman-Lehmann syndrome
Borjeson-Forssman-Lehmann syndrome 		9 0 2 5.6E-02 0 0
CUI: C0271091
Disease: Retinoschisis, Juvenile, X-Linked
Retinoschisis, Juvenile, X-Linked 		10 0 2 5.4E-02 0 0
CUI: C0522055
Disease: Electrocardiogram abnormal
Electrocardiogram abnormal 		11 0 2 5.3E-02 0 0
CUI: C0750403
Disease: Proximal weakness
Proximal weakness 		11 0 2 5.3E-02 0 0
CUI: C4743661
Disease: Leukocyte Adhesion Deficiency Type 3
Leukocyte Adhesion Deficiency Type 3 		11 0 2 5.3E-02 0 0
CUI: C0342513
Disease: Idiopathic hirsutism
Idiopathic hirsutism 		12 0 2 5.1E-02 0 0
CUI: C3542021
Disease: Duchenne and Becker Muscular Dystrophy
Duchenne and Becker Muscular Dystrophy 		12 0 2 5.1E-02 0 0
CUI: C4049650
Disease: Familial Glucocorticoid Deficiency Type 1
Familial Glucocorticoid Deficiency Type 1 		12 0 2 5.1E-02 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 6 5.1E-02 0 0
CUI: C0152439
Disease: Retinoschisis
Retinoschisis 		13 0 2 5.0E-02 0 0
CUI: C0877009
Disease: Muscle fibrosis
Muscle fibrosis 		34 0 3 5.0E-02 0 0