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: 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: C4310798
Disease: IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4 		1 0 1 0.33 0 0
CUI: C4310799
Disease: IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3 		1 0 1 0.33 0 0
CUI: C3279748
Disease: IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2 		2 0 1 0.25 0 0
CUI: C0410192
Disease: Muscular Dystrophy, Scapulohumeral
Muscular Dystrophy, Scapulohumeral 		3 0 1 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: C4551557
Disease: IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1 		3 15 1 0.20 1 6.7E-02
CUI: C1834671
Disease: FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B 		5 0 1 0.14 0 0
CUI: C0009451
Disease: Communicating Hydrocephalus
Communicating Hydrocephalus 		26 0 3 0.12 0 0
CUI: C0241442
Disease: Protrusion of tongue
Protrusion of tongue 		27 0 3 0.11 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: C4277512
Disease: Breast Cancer Lymphedema
Breast Cancer Lymphedema 		7 0 1 0.11 0 0
CUI: C1855204
Disease: Cellular immunodeficiency
Cellular immunodeficiency 		30 0 3 1.0E-01 0 0
CUI: C1399819
Disease: Humoral immunodeficiency
Humoral immunodeficiency 		9 0 1 9.1E-02 0 0
CUI: C4551705
Disease: Abnormality of chromosome stability
Abnormality of chromosome stability 		34 0 3 8.8E-02 0 0
CUI: C0023472
Disease: Leukemia, Myeloid, Accelerated Phase
Leukemia, Myeloid, Accelerated Phase 		12 0 1 7.1E-02 0 0
CUI: C1859447
Disease: Hypoplastic ischia
Hypoplastic ischia 		14 0 1 6.2E-02 0 0
CUI: C1656427
Disease: Early onset schizophrenia
Early onset schizophrenia 		15 0 1 5.9E-02 0 0
CUI: C2931322
Disease: T-Lymphocytopenia
T-Lymphocytopenia 		17 0 1 5.3E-02 0 0
CUI: C4316788
Disease: Abnormality of the intestine
Abnormality of the intestine 		19 0 1 4.8E-02 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 2 4.5E-02 0 0
CUI: C0003257
Disease: Antibody Deficiency Syndrome
Antibody Deficiency Syndrome 		21 0 1 4.3E-02 0 0
CUI: C0427515
Disease: Neutrophil abnormality
Neutrophil abnormality 		74 0 3 4.1E-02 0 0
CUI: C0011757
Disease: Developmental Coordination Disorder
Developmental Coordination Disorder 		23 0 1 4.0E-02 0 0