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: C0085668
Disease: Secondary carcinoma
Secondary carcinoma 		1 0 1 1.1E-02 0 0
CUI: C0149704
Disease: Gingivostomatitis
Gingivostomatitis 		1 0 1 1.1E-02 0 0
CUI: C0152497
Disease: Food poisoning caused by Vibrio parahaemolyticus
Food poisoning caused by Vibrio parahaemolyticus 		1 0 1 1.1E-02 0 0
CUI: C0153092
Disease: Mumps meningitis
Mumps meningitis 		1 0 1 1.1E-02 0 0
CUI: C0153261
Disease: Histoplasma capsulatum Infection
Histoplasma capsulatum Infection 		1 0 1 1.1E-02 0 0
CUI: C0154565
Disease: Non-organic sleep disorder
Non-organic sleep disorder 		1 0 1 1.1E-02 0 0
CUI: C0154834
Disease: Retinal Microaneurysm
Retinal Microaneurysm 		1 0 1 1.1E-02 0 0
CUI: C0154884
Disease: Acute posterior multifocal placoid pigment epitheliopathy
Acute posterior multifocal placoid pigment epitheliopathy 		1 0 1 1.1E-02 0 0
CUI: C0155563
Disease: Rheumatic mitral regurgitation
Rheumatic mitral regurgitation 		1 0 1 1.1E-02 0 0
CUI: C0155568
Disease: Rheumatic aortic regurgitation
Rheumatic aortic regurgitation 		1 0 1 1.1E-02 0 0
CUI: C0155804
Disease: Acute maxillary sinusitis
Acute maxillary sinusitis 		1 0 1 1.1E-02 0 0
CUI: C0156318
Disease: Fibrosclerosis of breast
Fibrosclerosis of breast 		1 0 1 1.1E-02 0 0
CUI: C0158543
Disease: Congenital cystic eyeball
Congenital cystic eyeball 		1 0 1 1.1E-02 0 0
CUI: C0221745
Disease: Depression suicidal
Depression suicidal 		1 0 1 1.1E-02 0 0
CUI: C0233594
Disease: Tail-biting
Tail-biting 		1 0 1 1.1E-02 0 0
CUI: C0236656
Disease: Dementia associated with alcoholism
Dementia associated with alcoholism 		1 0 1 1.1E-02 0 0
CUI: C0238517
Disease: Vaginal clear cell adenocarcinoma
Vaginal clear cell adenocarcinoma 		1 0 1 1.1E-02 0 0
CUI: C0240995
Disease: Increased serum androstenedione
Increased serum androstenedione 		1 0 1 1.1E-02 0 0
CUI: C0241518
Disease: Retraction of tympanic membrane
Retraction of tympanic membrane 		1 0 1 1.1E-02 0 0
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction 		1 1 1 1.1E-02 1 1.8E-02
CUI: C0263583
Disease: Idiopathic guttate hypomelanosis
Idiopathic guttate hypomelanosis 		1 0 1 1.1E-02 0 0
CUI: C0264622
Disease: Psychogenic voice disorder
Psychogenic voice disorder 		1 0 1 1.1E-02 0 0
CUI: C0266266
Disease: Congenital absence of pancreas
Congenital absence of pancreas 		1 0 1 1.1E-02 0 0
CUI: C0267095
Disease: Leukoplakia of esophagus
Leukoplakia of esophagus 		1 0 1 1.1E-02 0 0
CUI: C0267406
Disease: Mesenteric infarction
Mesenteric infarction 		1 0 1 1.1E-02 0 0