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: C0079584
Disease: Ichthyosis Vulgaris
Ichthyosis Vulgaris 		10 0 3 0.12 0 0
CUI: C0948825
Disease: Systremma
Systremma 		2 0 2 0.12 0 0
CUI: C0587044
Disease: Left ventricular thrombus
Left ventricular thrombus 		3 0 2 0.11 0 0
CUI: C1328551
Disease: Transfusion associated graft versus host disease
Transfusion associated graft versus host disease 		3 0 2 0.11 0 0
CUI: C3668940
Disease: Dmd-Associated Dilated Cardiomyopathy
Dmd-Associated Dilated Cardiomyopathy 		3 0 2 0.11 0 0
CUI: C1998045
Disease: Subclinical hyperthyroidism
Subclinical hyperthyroidism 		5 0 2 1.0E-01 0 0
CUI: C4554215
Disease: Duchenne or Becker muscular dystrophy
Duchenne or Becker muscular dystrophy 		7 0 2 9.1E-02 0 0
CUI: C0020758
Disease: Congenital ichthyosis
Congenital ichthyosis 		80 0 8 9.0E-02 0 0
CUI: C0154208
Disease: Disorder of endocrine ovary
Disorder of endocrine ovary 		22 0 3 8.3E-02 0 0
CUI: C0741933
Disease: cardiac symptom
cardiac symptom 		9 0 2 8.3E-02 0 0
CUI: C0079588
Disease: Ichthyosis, X-Linked
Ichthyosis, X-Linked 		199 0 16 8.0E-02 0 0
CUI: C0158447
Disease: Idiopathic osteoporosis
Idiopathic osteoporosis 		10 0 2 8.0E-02 0 0
CUI: C1963961
Disease: Testosterone deficiency
Testosterone deficiency 		24 0 3 7.9E-02 0 0
CUI: C0268263
Disease: Multiple Sulfatase Deficiency Disease
Multiple Sulfatase Deficiency Disease 		11 0 2 7.7E-02 0 0
CUI: C0948775
Disease: High weight
High weight 		12 0 2 7.4E-02 0 0
CUI: C3542021
Disease: Duchenne and Becker Muscular Dystrophy
Duchenne and Becker Muscular Dystrophy 		12 0 2 7.4E-02 0 0
CUI: C0152256
Disease: Disuse osteoporosis
Disuse osteoporosis 		13 0 2 7.1E-02 0 0
CUI: C0264733
Disease: Ventricular dilatation (disorder)
Ventricular dilatation (disorder) 		13 0 2 7.1E-02 0 0
CUI: C0016952
Disease: Galactosemias
Galactosemias 		29 0 3 7.0E-02 0 0
CUI: C1839783
Disease: Large forehead
Large forehead 		14 0 2 6.9E-02 0 0
CUI: C2931498
Disease: Mental Retardation, X-Linked 1
Mental Retardation, X-Linked 1 		45 0 4 6.9E-02 0 0
CUI: C0079583
Disease: Ichthyosiform Erythroderma, Congenital
Ichthyosiform Erythroderma, Congenital 		31 0 3 6.7E-02 0 0
CUI: C3839589
Disease: Secondary osteoporosis
Secondary osteoporosis 		15 0 2 6.7E-02 0 0
CUI: C0268151
Disease: Classical galactosemia
Classical galactosemia 		32 0 3 6.5E-02 0 0
CUI: C0008445
Disease: Chondrodysplasia Punctata
Chondrodysplasia Punctata 		16 0 2 6.5E-02 0 0