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: C0017412
Disease: Genital Diseases, Male
Genital Diseases, Male 		1 0 1 5.0E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 5.0E-02 0 0
CUI: C0235832
Disease: Congenital hernia
Congenital hernia 		1 0 1 5.0E-02 0 0
CUI: C0236099
Disease: Disorder of male reproductive system
Disorder of male reproductive system 		1 0 1 5.0E-02 0 0
CUI: C0266430
Disease: Polyorchism
Polyorchism 		1 0 1 5.0E-02 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 5.0E-02 0 0
CUI: C0342530
Disease: Incomplete testicular feminization syndrome
Incomplete testicular feminization syndrome 		1 0 1 5.0E-02 0 0
CUI: C0406482
Disease: Nodulocystic acne
Nodulocystic acne 		1 0 1 5.0E-02 0 0
CUI: C0406563
Disease: Follicular atrophoderma
Follicular atrophoderma 		1 0 1 5.0E-02 0 0
CUI: C0752353
Disease: Atrophy, Muscular, Spinobulbar
Atrophy, Muscular, Spinobulbar 		1 0 1 5.0E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 5.0E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 5.0E-02 0 0
CUI: C0860159
Disease: Partial androgen resistance
Partial androgen resistance 		1 0 1 5.0E-02 0 0
CUI: C0865181
Disease: Female Virilization
Female Virilization 		1 0 1 5.0E-02 0 0
CUI: C1266156
Disease: Multicystic mesothelioma, benign
Multicystic mesothelioma, benign 		1 0 1 5.0E-02 0 0
CUI: C1833699
Disease: Osteopoikilosis, Isolated
Osteopoikilosis, Isolated 		1 0 1 5.0E-02 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 5.0E-02 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 5.0E-02 0 0
CUI: C1835851
Disease: Ichthyosis with hypotrichosis, autosomal recessive
Ichthyosis with hypotrichosis, autosomal recessive 		1 0 1 5.0E-02 0 0
CUI: C1846010
Disease: URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME 		1 0 1 5.0E-02 0 0
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 11 1 5.0E-02 10 0.29
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 5.0E-02 0 0
CUI: C2584751
Disease: Severe hereditary factor VIII deficiency disease without inhibitor
Severe hereditary factor VIII deficiency disease without inhibitor 		1 0 1 5.0E-02 0 0
CUI: C2675074
Disease: Enlarged peripheral nerve
Enlarged peripheral nerve 		1 0 1 5.0E-02 0 0
CUI: C2678015
Disease: Myopathy, Reducing Body, X-Linked, Childhood-Onset
Myopathy, Reducing Body, X-Linked, Childhood-Onset 		1 0 1 5.0E-02 0 0