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: C4531166
Disease: Decreased lymphocyte proliferation in response to mitogen
Decreased lymphocyte proliferation in response to mitogen 		13 0 3 0.15 0 0
CUI: C1842714
Disease: Desquamation of skin soon after birth
Desquamation of skin soon after birth 		14 0 3 0.14 0 0
CUI: C1832323
Disease: Failure to thrive secondary to recurrent infections
Failure to thrive secondary to recurrent infections 		7 0 2 0.13 0 0
CUI: C4024599
Disease: Chronic oral candidiasis
Chronic oral candidiasis 		8 0 2 0.12 0 0
CUI: C4022983
Disease: Abnormal ciliary motility
Abnormal ciliary motility 		9 5 2 0.12 2 0.40
CUI: C4023438
Disease: Recurrent mycobacterial infections
Recurrent mycobacterial infections 		9 0 2 0.12 0 0
CUI: C1844384
Disease: Recurrent fungal infections
Recurrent fungal infections 		20 0 3 0.11 0 0
CUI: C1837066
Disease: Recurrent viral infection
Recurrent viral infection 		32 0 4 0.11 0 0
CUI: C0037280
Disease: Skin Diseases, Parasitic
Skin Diseases, Parasitic 		1 0 1 1.0E-01 0 0
CUI: C0155833
Disease: Hyperplasia of adenoids
Hyperplasia of adenoids 		1 0 1 1.0E-01 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta 		1 0 1 1.0E-01 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula 		1 0 1 1.0E-01 0 0
CUI: C0272236
Disease: Hyperimmunoglobulin M syndrome
Hyperimmunoglobulin M syndrome 		12 0 2 1.0E-01 0 0
CUI: C0477324
Disease: Other combined immunodeficiencies
Other combined immunodeficiencies 		1 0 1 1.0E-01 0 0
CUI: C1275128
Disease: Autosomal recessive hyperimmunoglobulin M syndrome
Autosomal recessive hyperimmunoglobulin M syndrome 		1 0 1 1.0E-01 0 0
CUI: C1302424
Disease: Plasma cell myeloma/plasmacytoma
Plasma cell myeloma/plasmacytoma 		1 0 1 1.0E-01 0 0
CUI: C1841686
Disease: Absent hallux
Absent hallux 		1 0 1 1.0E-01 0 0
CUI: C1855003
Disease: Bilateral postaxial polydactyly
Bilateral postaxial polydactyly 		1 0 1 1.0E-01 0 0
CUI: C1859458
Disease: Cleft vertebral arch
Cleft vertebral arch 		1 0 1 1.0E-01 0 0
CUI: C1859462
Disease: Absent knee epiphyses
Absent knee epiphyses 		1 0 1 1.0E-01 0 0
CUI: C1865372
Disease: Athabaskan severe combined immunodeficiency
Athabaskan severe combined immunodeficiency 		1 0 1 1.0E-01 0 0
CUI: C1865373
Disease: SEVERE COMBINED IMMUNODEFICIENCY, PARTIAL
SEVERE COMBINED IMMUNODEFICIENCY, PARTIAL 		1 0 1 1.0E-01 0 0
CUI: C1868111
Disease: Polydactyly, preaxial 4
Polydactyly, preaxial 4 		1 0 1 1.0E-01 0 0
CUI: C1968943
Disease: Rudimentary to absent tibiae
Rudimentary to absent tibiae 		1 0 1 1.0E-01 0 0
CUI: C2931320
Disease: T cell immunodeficiency primary
T cell immunodeficiency primary 		1 0 1 1.0E-01 0 0