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: C0014854
Disease: Esophageal diverticulum
Esophageal diverticulum 		1 0 1 5.6E-02 0 0
CUI: C0042818
Disease: Visual discomfort
Visual discomfort 		1 0 1 5.6E-02 0 0
CUI: C0156353
Disease: Uterovaginal prolapse
Uterovaginal prolapse 		1 0 1 5.6E-02 0 0
CUI: C0266429
Disease: Monorchism
Monorchism 		1 0 1 5.6E-02 0 0
CUI: C0406726
Disease: Orofaciodigital syndrome 3
Orofaciodigital syndrome 3 		1 0 1 5.6E-02 0 0
CUI: C0406727
Disease: Orofaciodigital syndrome 4
Orofaciodigital syndrome 4 		1 0 1 5.6E-02 0 0
CUI: C1842577
Disease: JOUBERT SYNDROME 2
JOUBERT SYNDROME 2 		1 0 1 5.6E-02 0 0
CUI: C1846722
Disease: Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies
Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies 		1 0 1 5.6E-02 0 0
CUI: C1855000
Disease: Agenesis of central incisor
Agenesis of central incisor 		1 0 1 5.6E-02 0 0
CUI: C1857587
Disease: Orstavik Lindemann Solberg syndrome
Orstavik Lindemann Solberg syndrome 		1 0 1 5.6E-02 0 0
CUI: C1860165
Disease: Pulmonary valve defects
Pulmonary valve defects 		1 0 1 5.6E-02 0 0
CUI: C1864148
Disease: MECKEL SYNDROME, TYPE 2
MECKEL SYNDROME, TYPE 2 		1 0 1 5.6E-02 0 0
CUI: C2748545
Disease: QUESTION MARK EARS, ISOLATED
QUESTION MARK EARS, ISOLATED 		1 0 1 5.6E-02 0 0
CUI: C2749019
Disease: JOUBERT SYNDROME 10 (disorder)
JOUBERT SYNDROME 10 (disorder) 		1 0 1 5.6E-02 0 0
CUI: C2931046
Disease: Heart defect, tongue hamartoma and polysyndactyly
Heart defect, tongue hamartoma and polysyndactyly 		1 0 1 5.6E-02 0 0
CUI: C2931889
Disease: Oral-facial-digital syndrome, type 2
Oral-facial-digital syndrome, type 2 		1 0 1 5.6E-02 0 0
CUI: C3150127
Disease: BARDET-BIEDL SYNDROME 15
BARDET-BIEDL SYNDROME 15 		1 0 1 5.6E-02 0 0
CUI: C3150834
Disease: LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6
LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6 		1 0 1 5.6E-02 0 0
CUI: C3277723
Disease: JOUBERT SYNDROME 12
JOUBERT SYNDROME 12 		1 0 1 5.6E-02 0 0
CUI: C3279899
Disease: Hydrolethalus Syndrome 2
Hydrolethalus Syndrome 2 		1 0 1 5.6E-02 0 0
CUI: C3553404
Disease: AURICULOCONDYLAR SYNDROME 2
AURICULOCONDYLAR SYNDROME 2 		1 0 1 5.6E-02 0 0
CUI: C3553758
Disease: JOUBERT SYNDROME 18
JOUBERT SYNDROME 18 		1 0 1 5.6E-02 0 0
CUI: C3554235
Disease: JOUBERT SYNDROME 20
JOUBERT SYNDROME 20 		1 0 1 5.6E-02 0 0
CUI: C3806516
Disease: Disproportionate shortening of the tibia
Disproportionate shortening of the tibia 		1 0 1 5.6E-02 0 0
CUI: C3809352
Disease: MECKEL SYNDROME, TYPE 11
MECKEL SYNDROME, TYPE 11 		1 0 1 5.6E-02 0 0