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: C0024622
Disease: Malignant neoplasm of retina
Malignant neoplasm of retina 		1 0 1 7.1E-02 0 0
CUI: C0042171
Disease: Uveoparotid Fever
Uveoparotid Fever 		1 0 1 7.1E-02 0 0
CUI: C0393602
Disease: Isolated cervical dystonia
Isolated cervical dystonia 		1 0 1 7.1E-02 0 0
CUI: C0545081
Disease: mantle lymphoma
mantle lymphoma 		1 0 1 7.1E-02 0 0
CUI: C0730364
Disease: Idiopathic polypoidal choroidal vasculopathy
Idiopathic polypoidal choroidal vasculopathy 		1 0 1 7.1E-02 0 0
CUI: C0748483
Disease: Salmonella bacteraemia
Salmonella bacteraemia 		1 0 1 7.1E-02 0 0
CUI: C0861199
Disease: Lymphoplasmacytoid immunocytoma
Lymphoplasmacytoid immunocytoma 		1 0 1 7.1E-02 0 0
CUI: C0861999
Disease: Centrocytic (mantle cell) lymphoma (Kiel classification)
Centrocytic (mantle cell) lymphoma (Kiel classification) 		1 0 1 7.1E-02 0 0
CUI: C1266046
Disease: Atypical follicular adenoma
Atypical follicular adenoma 		1 0 1 7.1E-02 0 0
CUI: C1333786
Disease: Gastric Precancerous Condition
Gastric Precancerous Condition 		1 0 1 7.1E-02 0 0
CUI: C1333940
Disease: Head and Neck Basaloid Carcinoma
Head and Neck Basaloid Carcinoma 		1 0 1 7.1E-02 0 0
CUI: C1334413
Disease: Low Grade Ductal Breast Carcinoma In Situ
Low Grade Ductal Breast Carcinoma In Situ 		1 0 1 7.1E-02 0 0
CUI: C1515107
Disease: Synchronous Bilateral Breast Carcinoma
Synchronous Bilateral Breast Carcinoma 		1 0 1 7.1E-02 0 0
CUI: C1843542
Disease: T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC
T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC 		1 0 1 7.1E-02 0 0
CUI: C1855861
Disease: Glycogen Storage Disease 0, Liver
Glycogen Storage Disease 0, Liver 		1 0 1 7.1E-02 0 0
CUI: C1859624
Disease: Defective B cell differentiation
Defective B cell differentiation 		1 0 1 7.1E-02 0 0
CUI: C2677096
Disease: SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11
SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11 		1 0 1 7.1E-02 0 0
CUI: C3151302
Disease: Chromosome 13q14 deletion syndrome
Chromosome 13q14 deletion syndrome 		1 0 1 7.1E-02 0 0
CUI: C3496177
Disease: Atypical psychosis
Atypical psychosis 		1 0 1 7.1E-02 0 0
CUI: C3805838
Disease: VON HIPPEL-LINDAU SYNDROME, MODIFIER OF
VON HIPPEL-LINDAU SYNDROME, MODIFIER OF 		1 0 1 7.1E-02 0 0
CUI: C3810481
Disease: MULTIPLE MYELOMA, t(11;14) TYPE, SUSCEPTIBILITY TO
MULTIPLE MYELOMA, t(11;14) TYPE, SUSCEPTIBILITY TO 		1 0 1 7.1E-02 0 0
CUI: C3825373
Disease: Hodgkin's disease in children
Hodgkin's disease in children 		1 0 1 7.1E-02 0 0
CUI: C3888458
Disease: Enterovirus myocarditis
Enterovirus myocarditis 		1 0 1 7.1E-02 0 0
CUI: C4021658
Disease: Abnormality of vitamin B12 metabolism
Abnormality of vitamin B12 metabolism 		1 0 1 7.1E-02 0 0
CUI: C4315963
Disease: Alveolar bone loss around teeth
Alveolar bone loss around teeth 		1 0 1 7.1E-02 0 0