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: C0015461
Disease: Facial Neoplasms
Facial Neoplasms 		1 0 1 5.0E-02 0 0
CUI: C0151463
Disease: Abscess of breast
Abscess of breast 		1 0 1 5.0E-02 0 0
CUI: C0265974
Disease: Birthmark
Birthmark 		1 0 1 5.0E-02 0 0
CUI: C0266094
Disease: Congenital macrocheilia
Congenital macrocheilia 		1 0 1 5.0E-02 0 0
CUI: C0267024
Disease: Hypertrophy of lip
Hypertrophy of lip 		1 0 1 5.0E-02 0 0
CUI: C0272256
Disease: Solitary Osseous Plasmacytoma
Solitary Osseous Plasmacytoma 		1 0 1 5.0E-02 0 0
CUI: C0278685
Disease: Stage I Ovarian Cancer AJCC v6 and v7
Stage I Ovarian Cancer AJCC v6 and v7 		1 0 1 5.0E-02 0 0
CUI: C0332972
Disease: Congenital vascular proliferation
Congenital vascular proliferation 		1 0 1 5.0E-02 0 0
CUI: C0349623
Disease: Primary Melanocytic Lesion of Meninges
Primary Melanocytic Lesion of Meninges 		1 0 1 5.0E-02 0 0
CUI: C0392178
Disease: Lipiduria
Lipiduria 		1 0 1 5.0E-02 0 0
CUI: C0393602
Disease: Isolated cervical dystonia
Isolated cervical dystonia 		1 0 1 5.0E-02 0 0
CUI: C0522035
Disease: Edema of the upper extremity
Edema of the upper extremity 		1 0 1 5.0E-02 0 0
CUI: C0730364
Disease: Idiopathic polypoidal choroidal vasculopathy
Idiopathic polypoidal choroidal vasculopathy 		1 0 1 5.0E-02 0 0
CUI: C0865573
Disease: Mitral disease
Mitral disease 		1 0 1 5.0E-02 0 0
CUI: C1335748
Disease: Renal Pelvis Adenocarcinoma
Renal Pelvis Adenocarcinoma 		1 0 1 5.0E-02 0 0
CUI: C1706559
Disease: Cornea verticillata
Cornea verticillata 		1 0 1 5.0E-02 0 0
CUI: C1832942
Disease: JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder) 		1 0 1 5.0E-02 0 0
CUI: C1843542
Disease: T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC
T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC 		1 0 1 5.0E-02 0 0
CUI: C1848795
Disease: GRAVES DISEASE, SUSCEPTIBILITY TO, 1
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 		1 0 1 5.0E-02 0 0
CUI: C1853102
Disease: Cerebrooculofacioskeletal Syndrome 2
Cerebrooculofacioskeletal Syndrome 2 		1 0 1 5.0E-02 0 0
CUI: C1857692
Disease: Venous varicosities of celiac and mesenteric vessels
Venous varicosities of celiac and mesenteric vessels 		1 0 1 5.0E-02 0 0
CUI: C1859624
Disease: Defective B cell differentiation
Defective B cell differentiation 		1 0 1 5.0E-02 0 0
CUI: C1970808
Disease: Xeroderma Pigmentosum B-Cockayne Syndrome
Xeroderma Pigmentosum B-Cockayne Syndrome 		1 0 1 5.0E-02 0 0
CUI: C2931029
Disease: Nevi flammei, familial multiple
Nevi flammei, familial multiple 		1 0 1 5.0E-02 0 0
CUI: C3161259
Disease: Pilar and trichilemmal cysts
Pilar and trichilemmal cysts 		1 0 1 5.0E-02 0 0