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: C1835828
Disease: Invasive Pneumococcal Disease, Recurrent Isolated, 1
Invasive Pneumococcal Disease, Recurrent Isolated, 1 		2 0 2 0.50 0 0
CUI: C0019250
Disease: Hereditary factor I deficiency disease
Hereditary factor I deficiency disease 		1 0 1 0.25 0 0
CUI: C1845073
Disease: INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2 (disorder)
INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2 (disorder) 		1 0 1 0.25 0 0
CUI: C1845919
Disease: Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema 		1 0 1 0.25 0 0
CUI: C2752039
Disease: HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3 		1 0 1 0.25 0 0
CUI: C3809523
Disease: MACULAR DEGENERATION, AGE-RELATED, 13
MACULAR DEGENERATION, AGE-RELATED, 13 		1 0 1 0.25 0 0
CUI: C4016436
Disease: MACULAR DEGENERATION, AGE-RELATED, 13, SUSCEPTIBILITY TO
MACULAR DEGENERATION, AGE-RELATED, 13, SUSCEPTIBILITY TO 		1 0 1 0.25 0 0
CUI: C4025314
Disease: Atrophic, patchy alopecia
Atrophic, patchy alopecia 		1 0 1 0.25 0 0
CUI: C4225596
Disease: INCONTINENTIA PIGMENTI, ATYPICAL
INCONTINENTIA PIGMENTI, ATYPICAL 		1 0 1 0.25 0 0
CUI: C4551695
Disease: Retinal vascular proliferation
Retinal vascular proliferation 		1 0 1 0.25 0 0
CUI: C1737260
Disease: Recurrent mycobacterium avium complex infections
Recurrent mycobacterium avium complex infections 		2 0 1 0.20 0 0
CUI: C1845117
Disease: Immunodeficiency without anhidrotic ectodermal dysplasia
Immunodeficiency without anhidrotic ectodermal dysplasia 		2 0 1 0.20 0 0
CUI: C1970879
Disease: ATYPICAL MYCOBACTERIOSIS, FAMILIAL, X-LINKED 1 (disorder)
ATYPICAL MYCOBACTERIOSIS, FAMILIAL, X-LINKED 1 (disorder) 		2 0 1 0.20 0 0
CUI: C4024862
Disease: Recurrent staphylococcal infections
Recurrent staphylococcal infections 		2 0 1 0.20 0 0
CUI: C1274879
Disease: Port-wine stain with oculocutaneous melanosis
Port-wine stain with oculocutaneous melanosis 		3 0 1 0.17 0 0
CUI: C1846008
Disease: HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH ECTODERMAL DYSPLASIA, HYPOHIDROTIC
HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH ECTODERMAL DYSPLASIA, HYPOHIDROTIC 		3 0 1 0.17 0 0
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant 		3 0 1 0.17 0 0
CUI: C2720289
Disease: ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY 		3 0 1 0.17 0 0
CUI: C4025672
Disease: Impaired memory B cell generation
Impaired memory B cell generation 		3 0 1 0.17 0 0
CUI: C0398795
Disease: Secondary immune deficiency disorder
Secondary immune deficiency disorder 		4 0 1 0.14 0 0
CUI: C0423428
Disease: Scarred macula
Scarred macula 		4 0 1 0.14 0 0
CUI: C1969222
Disease: Decreased serum complement factor H
Decreased serum complement factor H 		4 0 1 0.14 0 0
CUI: C0152259
Disease: Cataract secondary to ocular disorder
Cataract secondary to ocular disorder 		5 0 1 0.12 0 0
CUI: C0406612
Disease: Encephalocraniocutaneous lipomatosis
Encephalocraniocutaneous lipomatosis 		5 0 1 0.12 0 0
CUI: C0410740
Disease: Acquired deformity of finger
Acquired deformity of finger 		5 0 1 0.12 0 0