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: C0003708
Disease: Arachnoiditis
Arachnoiditis 		1 0 1 2.0E-02 0 0
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 2.0E-02 0 0
CUI: C0006897
Disease: Capillariasis
Capillariasis 		1 0 1 2.0E-02 0 0
CUI: C0017412
Disease: Genital Diseases, Male
Genital Diseases, Male 		1 0 1 2.0E-02 0 0
CUI: C0020413
Disease: Hymenolepiasis
Hymenolepiasis 		1 0 1 2.0E-02 0 0
CUI: C0150841
Disease: muscle pain or weakness
muscle pain or weakness 		1 0 1 2.0E-02 0 0
CUI: C0152073
Disease: Taenia saginata infection
Taenia saginata infection 		1 0 1 2.0E-02 0 0
CUI: C0155477
Disease: Tympanosclerosis involving other combination of structures
Tympanosclerosis involving other combination of structures 		1 0 1 2.0E-02 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 2.0E-02 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 2.0E-02 0 0
CUI: C0235832
Disease: Congenital hernia
Congenital hernia 		1 0 1 2.0E-02 0 0
CUI: C0236099
Disease: Disorder of male reproductive system
Disorder of male reproductive system 		1 0 1 2.0E-02 0 0
CUI: C0262477
Disease: Eye problem
Eye problem 		1 0 1 2.0E-02 0 0
CUI: C0264356
Disease: Childhood bronchiectasis
Childhood bronchiectasis 		1 0 1 2.0E-02 0 0
CUI: C0266430
Disease: Polyorchism
Polyorchism 		1 0 1 2.0E-02 0 0
CUI: C0268288
Disease: Mild steroid 21-hydroxylase deficiency
Mild steroid 21-hydroxylase deficiency 		1 0 1 2.0E-02 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 2.0E-02 0 0
CUI: C0268493
Disease: Ochronotic arthritis
Ochronotic arthritis 		1 0 1 2.0E-02 0 0
CUI: C0270250
Disease: Meconium peritonitis
Meconium peritonitis 		1 0 1 2.0E-02 0 0
CUI: C0278714
Disease: stage IV Wilms tumor
stage IV Wilms tumor 		1 0 1 2.0E-02 0 0
CUI: C0342530
Disease: Incomplete testicular feminization syndrome
Incomplete testicular feminization syndrome 		1 0 1 2.0E-02 0 0
CUI: C0342712
Disease: Disorder of branched-chain amino acid metabolism
Disorder of branched-chain amino acid metabolism 		1 0 1 2.0E-02 0 0
CUI: C0406482
Disease: Nodulocystic acne
Nodulocystic acne 		1 0 1 2.0E-02 0 0
CUI: C0409224
Disease: Ochronotic arthropathy
Ochronotic arthropathy 		1 0 1 2.0E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 2.0E-02 0 0