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: C0034088
Disease: Pulmonary Valve Insufficiency
Pulmonary Valve Insufficiency 		22 0 1 4.5E-02 0 0
CUI: C0034642
Disease: Rales
Rales 		23 0 1 4.3E-02 0 0
CUI: C4721952
Disease: Familial Idiopathic Pulmonary Fibrosis
Familial Idiopathic Pulmonary Fibrosis 		23 0 1 4.3E-02 0 0
CUI: C0022579
Disease: Keratoderma
Keratoderma 		24 0 1 4.2E-02 0 0
CUI: C1335475
Disease: Primary Carcinoma
Primary Carcinoma 		25 0 1 4.0E-02 0 0
CUI: C0241181
Disease: Fragile skin
Fragile skin 		26 0 1 3.8E-02 0 0
CUI: C0406709
Disease: Hay-Wells syndrome
Hay-Wells syndrome 		26 0 1 3.8E-02 0 0
CUI: C0410916
Disease: Neonatal Death
Neonatal Death 		27 0 1 3.7E-02 0 0
CUI: C1720824
Disease: Sudden Cardiac Arrest
Sudden Cardiac Arrest 		27 0 1 3.7E-02 0 0
CUI: C0011071
Disease: Sudden death
Sudden death 		30 0 1 3.3E-02 0 0
CUI: C0265998
Disease: ANONYCHIA
ANONYCHIA 		30 0 1 3.3E-02 0 0
CUI: C0030436
Disease: Parakeratosis
Parakeratosis 		31 0 1 3.2E-02 0 0
CUI: C1527303
Disease: Chronic Airflow Obstruction
Chronic Airflow Obstruction 		35 0 1 2.9E-02 0 0
CUI: C0085106
Disease: Familial benign pemphigus
Familial benign pemphigus 		36 0 1 2.8E-02 0 0
CUI: C0221270
Disease: Acanthosis
Acanthosis 		37 0 1 2.7E-02 0 0
CUI: C0266427
Disease: Testicular regression syndrome
Testicular regression syndrome 		37 0 1 2.7E-02 0 0
CUI: C0014742
Disease: Erythema Multiforme
Erythema Multiforme 		38 0 1 2.6E-02 0 0
CUI: C0022596
Disease: Palmoplantar Keratosis
Palmoplantar Keratosis 		39 0 1 2.6E-02 0 0
CUI: C0265004
Disease: Dilatation of aorta
Dilatation of aorta 		39 0 1 2.6E-02 0 0
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
Left ventricular noncompaction cardiomyopathy 		39 0 1 2.6E-02 0 0
CUI: C0343055
Disease: Generalized pustular psoriasis
Generalized pustular psoriasis 		43 0 1 2.3E-02 0 0
CUI: C0014527
Disease: Epidermolysis Bullosa
Epidermolysis Bullosa 		47 0 1 2.1E-02 0 0
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		47 0 1 2.1E-02 0 0
CUI: C0085786
Disease: Hamman-Rich syndrome
Hamman-Rich syndrome 		55 0 1 1.8E-02 0 0
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		56 0 1 1.8E-02 0 0