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: C0037932
Disease: Curvature of spine
Curvature of spine 		1 0 1 1.7E-02 0 0
CUI: C0041667
Disease: Underweight
Underweight 		1 0 1 1.7E-02 0 0
CUI: C0080310
Disease: Left Ventricular Function
Left Ventricular Function 		1 0 1 1.7E-02 0 0
CUI: C1832471
Disease: Renal dysplasia diffuse cystic
Renal dysplasia diffuse cystic 		1 0 1 1.7E-02 0 0
CUI: C1837615
Disease: Ciliary Dyskinesia, Primary, 5
Ciliary Dyskinesia, Primary, 5 		1 0 1 1.7E-02 0 0
CUI: C1837618
Disease: CILIARY DYSKINESIA, PRIMARY, 3
CILIARY DYSKINESIA, PRIMARY, 3 		1 26 1 1.7E-02 19 4.6E-02
CUI: C1844776
Disease: CONE-ROD DYSTROPHY, X-LINKED, 1
CONE-ROD DYSTROPHY, X-LINKED, 1 		1 0 1 1.7E-02 0 0
CUI: C1847554
Disease: CILIARY DYSKINESIA, PRIMARY, 2 (disorder)
CILIARY DYSKINESIA, PRIMARY, 2 (disorder) 		1 5 1 1.7E-02 3 7.4E-03
CUI: C1851967
Disease: DYSLEXIA, SUSCEPTIBILITY TO, 1
DYSLEXIA, SUSCEPTIBILITY TO, 1 		1 0 1 1.7E-02 0 0
CUI: C1854684
Disease: obsolete Congenital myopia
obsolete Congenital myopia 		1 0 1 1.7E-02 0 0
CUI: C1857519
Disease: Malformation of the hepatic ductal plate
Malformation of the hepatic ductal plate 		1 0 1 1.7E-02 0 0
CUI: C1969052
Disease: MECKEL SYNDROME, TYPE 5
MECKEL SYNDROME, TYPE 5 		1 0 1 1.7E-02 0 0
CUI: C1969053
Disease: JOUBERT SYNDROME 7
JOUBERT SYNDROME 7 		1 0 1 1.7E-02 0 0
CUI: C1970506
Disease: CILIARY DYSKINESIA, PRIMARY, 6
CILIARY DYSKINESIA, PRIMARY, 6 		1 0 1 1.7E-02 0 0
CUI: C2024891
Disease: Reduced exercise tolerance
Reduced exercise tolerance 		1 0 1 1.7E-02 0 0
CUI: C2675228
Disease: CILIARY DYSKINESIA, PRIMARY, 12
CILIARY DYSKINESIA, PRIMARY, 12 		1 2 1 1.7E-02 1 2.5E-03
CUI: C2675229
Disease: CILIARY DYSKINESIA, PRIMARY, 11
CILIARY DYSKINESIA, PRIMARY, 11 		1 8 1 1.7E-02 4 9.9E-03
CUI: C2675867
Disease: CILIARY DYSKINESIA, PRIMARY, 10
CILIARY DYSKINESIA, PRIMARY, 10 		1 0 1 1.7E-02 0 0
CUI: C2676235
Disease: CILIARY DYSKINESIA, PRIMARY, 9
CILIARY DYSKINESIA, PRIMARY, 9 		1 2 1 1.7E-02 1 2.5E-03
CUI: C2749019
Disease: JOUBERT SYNDROME 10 (disorder)
JOUBERT SYNDROME 10 (disorder) 		1 0 1 1.7E-02 0 0
CUI: C2749137
Disease: Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness 		1 0 1 1.7E-02 0 0
CUI: C2750161
Disease: Absent/shortened outer dynein arms
Absent/shortened outer dynein arms 		1 0 1 1.7E-02 0 0
CUI: C2750790
Disease: CILIARY DYSKINESIA, PRIMARY, 13
CILIARY DYSKINESIA, PRIMARY, 13 		1 5 1 1.7E-02 3 7.4E-03
CUI: C3151137
Disease: CILIARY DYSKINESIA, PRIMARY, 15
CILIARY DYSKINESIA, PRIMARY, 15 		1 6 1 1.7E-02 4 9.9E-03
CUI: C3151460
Disease: CILIARY DYSKINESIA, PRIMARY, 16
CILIARY DYSKINESIA, PRIMARY, 16 		1 2 1 1.7E-02 2 5.0E-03