Source: CURATED ×
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: C2700553
Disease: Omenn Syndrome
Omenn Syndrome 		19 44 16 0.70 2 2.9E-02
CUI: C0242583
Disease: Bare Lymphocyte Syndrome
Bare Lymphocyte Syndrome 		6 0 6 0.30 0 0
CUI: C0700216
Disease: Structural Clinical Interview for DSM-III
Structural Clinical Interview for DSM-III 		5 0 5 0.25 0 0
CUI: C2931884
Disease: Reticuloendotheliosis, familial, with eosinophilia
Reticuloendotheliosis, familial, with eosinophilia 		3 0 3 0.15 0 0
CUI: C0494261
Disease: Combined immunodeficiency
Combined immunodeficiency 		41 10 7 0.13 3 8.8E-02
CUI: C1832322
Disease: Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive 		2 32 2 1.0E-01 2 3.5E-02
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 		2 14 2 1.0E-01 1 2.5E-02
CUI: C1865370
Disease: Severe combined immunodeficiency with sensitivity to ionizing radiation
Severe combined immunodeficiency with sensitivity to ionizing radiation 		2 0 2 1.0E-01 0 0
CUI: C1867362
Disease: SEVERE COMBINED IMMUNODEFICIENCY, B CELL-NEGATIVE
SEVERE COMBINED IMMUNODEFICIENCY, B CELL-NEGATIVE 		2 0 2 1.0E-01 0 0
CUI: C2673536
Disease: Combined Cellular And Humoral Immune Defects With Granulomas
Combined Cellular And Humoral Immune Defects With Granulomas 		2 19 2 1.0E-01 1 2.2E-02
CUI: C0003257
Disease: Antibody Deficiency Syndrome
Antibody Deficiency Syndrome 		17 0 2 5.7E-02 0 0
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder 		19 0 2 5.4E-02 0 0
CUI: C0003756
Disease: Arenaviridae Infections
Arenaviridae Infections 		1 0 1 5.0E-02 0 0
CUI: C0205671
Disease: Infections, Arenavirus
Infections, Arenavirus 		1 0 1 5.0E-02 0 0
CUI: C0238801
Disease: Bone marrow megaloblastic (finding)
Bone marrow megaloblastic (finding) 		1 0 1 5.0E-02 0 0
CUI: C0267537
Disease: Typhlitis
Typhlitis 		1 0 1 5.0E-02 0 0
CUI: C0268124
Disease: Adenosine deaminase deficiency
Adenosine deaminase deficiency 		1 0 1 5.0E-02 0 0
CUI: C0272167
Disease: Reticular dysgenesis
Reticular dysgenesis 		1 0 1 5.0E-02 0 0
CUI: C0342701
Disease: Transcobalamin II deficiency
Transcobalamin II deficiency 		1 0 1 5.0E-02 0 0
CUI: C0392607
Disease: Severe combined immunodeficiency due to adenosine deaminase deficiency
Severe combined immunodeficiency due to adenosine deaminase deficiency 		1 12 1 5.0E-02 2 5.4E-02
CUI: C0400823
Disease: Neutropenic colitis
Neutropenic colitis 		1 0 1 5.0E-02 0 0
CUI: C1279481
Disease: X-Linked Combined Immunodeficiency Diseases
X-Linked Combined Immunodeficiency Diseases 		1 40 1 5.0E-02 1 1.5E-02
CUI: C1282908
Disease: De Vaal's syndrome
De Vaal's syndrome 		1 0 1 5.0E-02 0 0
CUI: C1833275
Disease: Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative 		1 5 1 5.0E-02 1 3.2E-02
CUI: C1835407
Disease: HEPATITIS C VIRUS, SUSCEPTIBILITY TO
HEPATITIS C VIRUS, SUSCEPTIBILITY TO 		1 0 1 5.0E-02 0 0