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: C3279748
Disease: IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2 		2 0 2 0.67 0 0
CUI: C0494266
Disease: Other specified immunodeficiencies
Other specified immunodeficiencies 		1 0 1 0.33 0 0
CUI: C0857362
Disease: Groin nodes
Groin nodes 		1 0 1 0.33 0 0
CUI: C1333044
Disease: Chronic Myelomonocytic Leukemia-2
Chronic Myelomonocytic Leukemia-2 		1 0 1 0.33 0 0
CUI: C1835407
Disease: HEPATITIS C VIRUS, SUSCEPTIBILITY TO
HEPATITIS C VIRUS, SUSCEPTIBILITY TO 		1 0 1 0.33 0 0
CUI: C4330613
Disease: Burkitt-Like Lymphoma with 11q Aberration
Burkitt-Like Lymphoma with 11q Aberration 		2 0 1 0.25 0 0
CUI: C0398788
Disease: Immunodeficiency syndrome, variable
Immunodeficiency syndrome, variable 		3 1 1 0.20 1 6.7E-02
CUI: C0410192
Disease: Muscular Dystrophy, Scapulohumeral
Muscular Dystrophy, Scapulohumeral 		3 0 1 0.20 0 0
CUI: C1335684
Disease: Rectal Lipoma
Rectal Lipoma 		3 0 1 0.20 0 0
CUI: C1399819
Disease: Humoral immunodeficiency
Humoral immunodeficiency 		9 0 2 0.20 0 0
CUI: C1855767
Disease: Reduced natural killer cell count
Reduced natural killer cell count 		3 0 1 0.20 0 0
CUI: C0302329
Disease: Malignant lymphoma centroblastic, diffuse
Malignant lymphoma centroblastic, diffuse 		4 0 1 0.17 0 0
CUI: C1837028
Disease: Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive 		4 0 1 0.17 0 0
CUI: C1834671
Disease: FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B 		5 0 1 0.14 0 0
CUI: C1960273
Disease: Lymphocytic myocarditis
Lymphocytic myocarditis 		5 0 1 0.14 0 0
CUI: C0009759
Disease: Conjunctival Diseases
Conjunctival Diseases 		6 0 1 0.12 0 0
CUI: C1837873
Disease: LEBER CONGENITAL AMAUROSIS 9 (disorder)
LEBER CONGENITAL AMAUROSIS 9 (disorder) 		6 0 1 0.12 0 0
CUI: C4728223
Disease: Extramedullary myeloma
Extramedullary myeloma 		6 0 1 0.12 0 0
CUI: C0796113
Disease: Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor 		7 0 1 0.11 0 0
CUI: C1832323
Disease: Failure to thrive secondary to recurrent infections
Failure to thrive secondary to recurrent infections 		7 0 1 0.11 0 0
CUI: C2931322
Disease: T-Lymphocytopenia
T-Lymphocytopenia 		17 0 2 0.11 0 0
CUI: C4277512
Disease: Breast Cancer Lymphedema
Breast Cancer Lymphedema 		7 0 1 0.11 0 0
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		8 0 1 1.0E-01 0 0
CUI: C0019624
Disease: Histiocytosis, Non-Langerhans-Cell
Histiocytosis, Non-Langerhans-Cell 		9 0 1 9.1E-02 0 0
CUI: C1832324
Disease: Recurrent opportunistic infections
Recurrent opportunistic infections 		10 0 1 8.3E-02 0 0