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: C0042818
Disease: Visual discomfort
Visual discomfort 		1 0 1 5.3E-02 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta 		1 0 1 5.3E-02 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula 		1 0 1 5.3E-02 0 0
CUI: C0406726
Disease: Orofaciodigital syndrome 3
Orofaciodigital syndrome 3 		1 0 1 5.3E-02 0 0
CUI: C0431879
Disease: Brachymesophalangia
Brachymesophalangia 		1 0 1 5.3E-02 0 0
CUI: C1841686
Disease: Absent hallux
Absent hallux 		1 0 1 5.3E-02 0 0
CUI: C1849700
Disease: Hyperphenylalaninemia with primapterinuria
Hyperphenylalaninemia with primapterinuria 		1 0 1 5.3E-02 0 0
CUI: C1855003
Disease: Bilateral postaxial polydactyly
Bilateral postaxial polydactyly 		1 0 1 5.3E-02 0 0
CUI: C1855861
Disease: Glycogen Storage Disease 0, Liver
Glycogen Storage Disease 0, Liver 		1 0 1 5.3E-02 0 0
CUI: C1868111
Disease: Polydactyly, preaxial 4
Polydactyly, preaxial 4 		1 0 1 5.3E-02 0 0
CUI: C1868118
Disease: Orofaciodigital syndrome 5
Orofaciodigital syndrome 5 		1 0 1 5.3E-02 0 0
CUI: C1968943
Disease: Rudimentary to absent tibiae
Rudimentary to absent tibiae 		1 0 1 5.3E-02 0 0
CUI: C2053435
Disease: Absent cupid's bow
Absent cupid's bow 		1 0 1 5.3E-02 0 0
CUI: C2749019
Disease: JOUBERT SYNDROME 10 (disorder)
JOUBERT SYNDROME 10 (disorder) 		1 0 1 5.3E-02 0 0
CUI: C3280203
Disease: WARBURG MICRO SYNDROME 3
WARBURG MICRO SYNDROME 3 		1 0 1 5.3E-02 0 0
CUI: C3554235
Disease: JOUBERT SYNDROME 20
JOUBERT SYNDROME 20 		1 0 1 5.3E-02 0 0
CUI: C3809352
Disease: MECKEL SYNDROME, TYPE 11
MECKEL SYNDROME, TYPE 11 		1 0 1 5.3E-02 0 0
CUI: C3810265
Disease: WARBURG MICRO SYNDROME 4
WARBURG MICRO SYNDROME 4 		1 0 1 5.3E-02 0 0
CUI: C3810376
Disease: PREMATURE OVARIAN FAILURE 9
PREMATURE OVARIAN FAILURE 9 		1 0 1 5.3E-02 0 0
CUI: C3889474
Disease: BARDET-BIEDL SYNDROME 16
BARDET-BIEDL SYNDROME 16 		1 0 1 5.3E-02 0 0
CUI: C4014780
Disease: OROFACIODIGITAL SYNDROME XIV
OROFACIODIGITAL SYNDROME XIV 		1 0 1 5.3E-02 0 0
CUI: C4016298
Disease: POSTAXIAL POLYDACTYLY, TYPE A1/B
POSTAXIAL POLYDACTYLY, TYPE A1/B 		1 0 1 5.3E-02 0 0
CUI: C4016299
Disease: GREIG CEPHALOPOLYSYNDACTYLY SYNDROME, SEVERE
GREIG CEPHALOPOLYSYNDACTYLY SYNDROME, SEVERE 		1 0 1 5.3E-02 0 0
CUI: C4021072
Disease: Agenesis of canine
Agenesis of canine 		1 0 1 5.3E-02 0 0
CUI: C4021235
Disease: 1-5 toe syndactyly
1-5 toe syndactyly 		1 0 1 5.3E-02 0 0