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 1.00 0 0
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2
2 0 1 0.50 0 0
CUI: C0398788
Disease: Immunodeficiency syndrome, variable
Immunodeficiency syndrome, variable
3 0 1 0.33 0 0
CUI: C0410192
Disease: Muscular Dystrophy, Scapulohumeral
Muscular Dystrophy, Scapulohumeral
3 0 1 0.33 0 0
CUI: C1855767
Disease: Reduced natural killer cell count
Reduced natural killer cell count
3 0 1 0.33 0 0
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1
3 0 1 0.33 0 0
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B
5 0 1 0.20 0 0
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor
7 0 1 0.14 0 0
CUI: C4277512
Disease: Breast Cancer Lymphedema
Breast Cancer Lymphedema
7 0 1 0.14 0 0
CUI: C1399819
Disease: Humoral immunodeficiency
Humoral immunodeficiency
9 0 1 0.11 0 0
Leukemia, Myeloid, Accelerated Phase
12 0 1 8.3E-02 0 0
CUI: C1656427
Disease: Early onset schizophrenia
Early onset schizophrenia
15 0 1 6.7E-02 0 0
CUI: C2931322
Disease: T-Lymphocytopenia
T-Lymphocytopenia
17 0 1 5.9E-02 0 0
CUI: C0003257
Disease: Antibody Deficiency Syndrome
Antibody Deficiency Syndrome
21 0 1 4.8E-02 0 0
CUI: C0011757
Disease: Developmental Coordination Disorder
Developmental Coordination Disorder
23 0 1 4.3E-02 0 0
Stage III Cutaneous Melanoma AJCC v6
24 0 1 4.2E-02 0 0
CUI: C4745063
Disease: Biliary Tract Carcinoma
Biliary Tract Carcinoma
25 0 1 4.0E-02 0 0
CUI: C0009451
Disease: Communicating Hydrocephalus
Communicating Hydrocephalus
26 0 1 3.8E-02 0 0
CUI: C0241442
Disease: Protrusion of tongue
Protrusion of tongue
27 0 1 3.7E-02 0 0
CUI: C0522274
Disease: Humoral immune defect
Humoral immune defect
29 0 1 3.4E-02 0 0
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation
29 0 1 3.4E-02 0 0
CUI: C1335059
Disease: testicular nonseminoma
testicular nonseminoma
30 0 1 3.3E-02 0 0
CUI: C1855204
Disease: Cellular immunodeficiency
Cellular immunodeficiency
30 0 1 3.3E-02 0 0
Temporomandibular joint osteoarthritis
32 0 1 3.1E-02 0 0
CUI: C4551705
Disease: Abnormality of chromosome stability
Abnormality of chromosome stability
34 0 1 2.9E-02 0 0