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: C2717884
Disease: Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant 		4 0 4 0.29 0 0
CUI: C1858969
Disease: Decreased lymphocyte apoptosis
Decreased lymphocyte apoptosis 		5 0 4 0.27 0 0
CUI: C2674723
Disease: RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER 		6 0 4 0.25 0 0
CUI: C0220679
Disease: Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified
Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified 		3 0 3 0.21 0 0
CUI: C4021962
Disease: Genital hernia
Genital hernia 		3 0 3 0.21 0 0
CUI: C4703376
Disease: Increased proportion of HLA DR+ T cells
Increased proportion of HLA DR+ T cells 		3 0 3 0.21 0 0
CUI: C0241185
Disease: Smooth muscle antibodies positive
Smooth muscle antibodies positive 		4 0 3 0.20 0 0
CUI: C0268336
Disease: Ehlers-Danlos syndrome type 2
Ehlers-Danlos syndrome type 2 		4 0 3 0.20 0 0
CUI: C1843386
Disease: Reduced delayed hypersensitivity
Reduced delayed hypersensitivity 		4 0 3 0.20 0 0
CUI: C1858980
Disease: Platelet antibody positive
Platelet antibody positive 		4 0 3 0.20 0 0
CUI: C4538407
Disease: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2 		4 37 3 0.20 1 2.6E-02
CUI: C4014733
Disease: Follicular hyperplasia
Follicular hyperplasia 		11 0 4 0.19 0 0
CUI: C1858972
Disease: Increased B cell count
Increased B cell count 		5 0 3 0.19 0 0
CUI: C1858973
Disease: Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells
Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells 		5 0 3 0.19 0 0
CUI: C4021032
Disease: Abnormal vitamin B12 level
Abnormal vitamin B12 level 		5 0 3 0.19 0 0
CUI: C4531156
Disease: Abnormal proportion of CD4 T cells
Abnormal proportion of CD4 T cells 		5 0 3 0.19 0 0
CUI: C4552122
Disease: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 		5 81 3 0.19 1 1.2E-02
CUI: C0520736
Disease: Coombs positive hemolytic anemia
Coombs positive hemolytic anemia 		6 0 3 0.18 0 0
CUI: C4021747
Disease: Specific anti-polysaccharide antibody deficiency
Specific anti-polysaccharide antibody deficiency 		6 0 3 0.18 0 0
CUI: C4280772
Disease: Abnormal serum interleukin level
Abnormal serum interleukin level 		6 0 3 0.18 0 0
CUI: C4531155
Disease: Abnormal proportion of CD8 T cells
Abnormal proportion of CD8 T cells 		6 0 3 0.18 0 0
CUI: C0151379
Disease: Rheumatoid factor positive (finding)
Rheumatoid factor positive (finding) 		7 0 3 0.17 0 0
CUI: C0432363
Disease: Shagreen patch
Shagreen patch 		8 0 3 0.16 0 0
CUI: C0575484
Disease: Long thorax
Long thorax 		9 0 3 0.15 0 0
CUI: C3887531
Disease: Keratoglobus
Keratoglobus 		9 0 3 0.15 0 0