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: C0521707
Disease: Bilateral cataracts (disorder)
Bilateral cataracts (disorder)
0 37 0 0 1 9.9E-03
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia
0 1 0 0 1 1.5E-02
CUI: C1833999
Disease: Retinal pigmentary degeneration
Retinal pigmentary degeneration
1 0 1 5.0E-02 0 0
Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies
1 0 1 5.0E-02 0 0
CUI: C1853153
Disease: JOUBERT SYNDROME 6
JOUBERT SYNDROME 6
1 48 1 5.0E-02 2 1.8E-02
CUI: C1857587
Disease: Orstavik Lindemann Solberg syndrome
Orstavik Lindemann Solberg syndrome
1 0 1 5.0E-02 0 0
CUI: C1857780
Disease: JOUBERT SYNDROME 5
JOUBERT SYNDROME 5
1 0 1 5.0E-02 0 0
LEBER CONGENITAL AMAUROSIS 10 (disorder)
1 0 1 5.0E-02 0 0
CUI: C1858054
Disease: BARDET-BIEDL SYNDROME 6
BARDET-BIEDL SYNDROME 6
1 21 1 5.0E-02 1 1.2E-02
CUI: C1859565
Disease: BARDET-BIEDL SYNDROME 7
BARDET-BIEDL SYNDROME 7
1 0 1 5.0E-02 0 0
CUI: C1859566
Disease: BARDET-BIEDL SYNDROME 8
BARDET-BIEDL SYNDROME 8
1 0 1 5.0E-02 0 0
CUI: C1859567
Disease: BARDET-BIEDL SYNDROME 9
BARDET-BIEDL SYNDROME 9
1 11 1 5.0E-02 1 1.3E-02
CUI: C1859568
Disease: BARDET-BIEDL SYNDROME 10
BARDET-BIEDL SYNDROME 10
1 94 1 5.0E-02 3 1.9E-02
CUI: C1859570
Disease: BARDET-BIEDL SYNDROME 12
BARDET-BIEDL SYNDROME 12
1 0 1 5.0E-02 0 0
CUI: C1860165
Disease: Pulmonary valve defects
Pulmonary valve defects
1 0 1 5.0E-02 0 0
CUI: C1970161
Disease: MECKEL SYNDROME, TYPE 4
MECKEL SYNDROME, TYPE 4
1 0 1 5.0E-02 0 0
Heart defect, tongue hamartoma and polysyndactyly
1 0 1 5.0E-02 0 0
CUI: C3150127
Disease: BARDET-BIEDL SYNDROME 15
BARDET-BIEDL SYNDROME 15
1 0 1 5.0E-02 0 0
CUI: C3150715
Disease: RETINITIS PIGMENTOSA 51
RETINITIS PIGMENTOSA 51
1 0 1 5.0E-02 0 0
CUI: C3150796
Disease: NEPHRONOPHTHISIS 11
NEPHRONOPHTHISIS 11
1 6 1 5.0E-02 1 1.4E-02
CUI: C3150808
Disease: RETINITIS PIGMENTOSA 55
RETINITIS PIGMENTOSA 55
1 0 1 5.0E-02 0 0
CUI: C3277723
Disease: JOUBERT SYNDROME 12
JOUBERT SYNDROME 12
1 0 1 5.0E-02 0 0
CUI: C3279899
Disease: Hydrolethalus Syndrome 2
Hydrolethalus Syndrome 2
1 0 1 5.0E-02 0 0
CUI: C4016435
Disease: BARDET-BIEDL SYNDROME 1/7, DIGENIC
BARDET-BIEDL SYNDROME 1/7, DIGENIC
1 0 1 5.0E-02 0 0
CUI: C4016957
Disease: BARDET-BIEDL SYNDROME 1/2, DIGENIC
BARDET-BIEDL SYNDROME 1/2, DIGENIC
1 0 1 5.0E-02 0 0