Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Anti-polysaccharide antibody deficiency
1 0 1 1.00 0 0
Autosomal agammaglobulinemia with absent B-cells
1 0 1 1.00 0 0
CUI: C0746757
Disease: Chronic nasal congestion
Chronic nasal congestion
1 0 1 1.00 0 0
CUI: C1843995
Disease: Enteroviral hepatitis
Enteroviral hepatitis
1 0 1 1.00 0 0
CUI: C3203655
Disease: Autoimmune aplastic anaemia
Autoimmune aplastic anaemia
1 0 1 1.00 0 0
Enteroviral dermatomyositis syndrome
1 0 1 1.00 0 0
AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE
2 0 1 0.50 0 0
CUI: C4087393
Disease: Marginal zone lymphoma refractory
Marginal zone lymphoma refractory
2 0 1 0.50 0 0
Recurrent Hemophagocytic Lymphohistiocytosis
2 0 1 0.50 0 0
CUI: C0008684
Disease: Chronic gingivitis
Chronic gingivitis
3 0 1 0.33 0 0
CUI: C0270710
Disease: Bing-Neel syndrome
Bing-Neel syndrome
3 0 1 0.33 0 0
Vaccine associated paralytic poliomyelitis
3 0 1 0.33 0 0
CUI: C0241932
Disease: X-linked hypogammaglobulinemia
X-linked hypogammaglobulinemia
4 0 1 0.25 0 0
CUI: C4025683
Disease: Lymph node hypoplasia
Lymph node hypoplasia
4 0 1 0.25 0 0
CUI: C4025681
Disease: Recurrent enteroviral infections
Recurrent enteroviral infections
5 0 1 0.20 0 0
CUI: C0855138
Disease: Mantle cell lymphoma refractory
Mantle cell lymphoma refractory
6 0 1 0.17 0 0
CUI: C1863715
Disease: Severe B lymphocytopenia
Severe B lymphocytopenia
6 0 1 0.17 0 0
Recurrent cutaneous abscess formation
6 0 1 0.17 0 0
CUI: C0034212
Disease: Pyoderma
Pyoderma
7 0 1 0.14 0 0
Autosomal recessive agammaglobulinemia
7 0 1 0.14 0 0
CUI: C0014534
Disease: Epididymitis
Epididymitis
8 0 1 0.12 0 0
CUI: C0745242
Disease: Immunoglobulin deficiency
Immunoglobulin deficiency
8 0 1 0.12 0 0
CUI: C3888789
Disease: Pancreatic toxicity
Pancreatic toxicity
8 0 1 0.12 0 0
CUI: C1399819
Disease: Humoral immunodeficiency
Humoral immunodeficiency
9 0 1 0.11 0 0
CUI: C0162539
Disease: IgG Deficiency disorder
IgG Deficiency disorder
10 0 1 1.0E-01 0 0