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: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		0 61 0 0 1 1.2E-02
CUI: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 1.4E-02 0 0
CUI: C0006542
Disease: Byssinosis
Byssinosis 		1 0 1 1.4E-02 0 0
CUI: C0024950
Disease: Maxillary Diseases
Maxillary Diseases 		1 0 1 1.4E-02 0 0
CUI: C0029437
Disease: Idiopathic Multicentric Osteolyses
Idiopathic Multicentric Osteolyses 		1 0 1 1.4E-02 0 0
CUI: C0029896
Disease: Otorhinolaryngologic Diseases
Otorhinolaryngologic Diseases 		1 0 1 1.4E-02 0 0
CUI: C0030328
Disease: Panniculitis, Nodular Nonsuppurative
Panniculitis, Nodular Nonsuppurative 		1 0 1 1.4E-02 0 0
CUI: C0086492
Disease: J-Pouch
J-Pouch 		1 0 1 1.4E-02 0 0
CUI: C0149704
Disease: Gingivostomatitis
Gingivostomatitis 		1 0 1 1.4E-02 0 0
CUI: C0153470
Disease: Malignant neoplasm of spleen
Malignant neoplasm of spleen 		1 0 1 1.4E-02 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea 		1 0 1 1.4E-02 0 0
CUI: C0155563
Disease: Rheumatic mitral regurgitation
Rheumatic mitral regurgitation 		1 0 1 1.4E-02 0 0
CUI: C0241518
Disease: Retraction of tympanic membrane
Retraction of tympanic membrane 		1 0 1 1.4E-02 0 0
CUI: C0241876
Disease: Obstructive emphysema
Obstructive emphysema 		1 0 1 1.4E-02 0 0
CUI: C0263583
Disease: Idiopathic guttate hypomelanosis
Idiopathic guttate hypomelanosis 		1 0 1 1.4E-02 0 0
CUI: C0264955
Disease: Idiopathic arterial calcification of infancy
Idiopathic arterial calcification of infancy 		1 0 1 1.4E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 1.4E-02 0 0
CUI: C0265988
Disease: Congenital accessory skin tag
Congenital accessory skin tag 		1 0 1 1.4E-02 0 0
CUI: C0266266
Disease: Congenital absence of pancreas
Congenital absence of pancreas 		1 0 1 1.4E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 1.4E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 1.4E-02 0 0
CUI: C0269014
Disease: Fibrosis of corpus cavernosum
Fibrosis of corpus cavernosum 		1 0 1 1.4E-02 0 0
CUI: C0270075
Disease: Perinatal disorder
Perinatal disorder 		1 0 1 1.4E-02 0 0
CUI: C0333295
Disease: Acute ulcer
Acute ulcer 		1 0 1 1.4E-02 0 0
CUI: C0338822
Disease: Cycloid psychosis
Cycloid psychosis 		1 0 1 1.4E-02 0 0