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: C0080310
Disease: Left Ventricular Function
Left Ventricular Function 		1 0 1 3.3E-02 0 0
CUI: C0158611
Disease: Other congenital anomalies of heart
Other congenital anomalies of heart 		1 2 1 3.3E-02 2 0.12
CUI: C0266632
Disease: Ectopic spleen
Ectopic spleen 		1 0 1 3.3E-02 0 0
CUI: C0267581
Disease: Rectal Stenosis
Rectal Stenosis 		1 0 1 3.3E-02 0 0
CUI: C0344923
Disease: Multiple ventricular septal defects
Multiple ventricular septal defects 		1 0 1 3.3E-02 0 0
CUI: C0478009
Disease: Congenital malformation of cardiac chambers and connections, unspecified
Congenital malformation of cardiac chambers and connections, unspecified 		1 2 1 3.3E-02 2 0.12
CUI: C0796102
Disease: Orofaciodigital syndrome 9
Orofaciodigital syndrome 9 		1 0 1 3.3E-02 0 0
CUI: C1833999
Disease: Retinal pigmentary degeneration
Retinal pigmentary degeneration 		1 0 1 3.3E-02 0 0
CUI: C1837618
Disease: CILIARY DYSKINESIA, PRIMARY, 3
CILIARY DYSKINESIA, PRIMARY, 3 		1 0 1 3.3E-02 0 0
CUI: C1847554
Disease: CILIARY DYSKINESIA, PRIMARY, 2 (disorder)
CILIARY DYSKINESIA, PRIMARY, 2 (disorder) 		1 0 1 3.3E-02 0 0
CUI: C1853153
Disease: JOUBERT SYNDROME 6
JOUBERT SYNDROME 6 		1 0 1 3.3E-02 0 0
CUI: C1854684
Disease: obsolete Congenital myopia
obsolete Congenital myopia 		1 0 1 3.3E-02 0 0
CUI: C1857780
Disease: JOUBERT SYNDROME 5
JOUBERT SYNDROME 5 		1 0 1 3.3E-02 0 0
CUI: C1857821
Disease: LEBER CONGENITAL AMAUROSIS 10 (disorder)
LEBER CONGENITAL AMAUROSIS 10 (disorder) 		1 0 1 3.3E-02 0 0
CUI: C1858535
Disease: MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 2 (disorder)
MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 2 (disorder) 		1 0 1 3.3E-02 0 0
CUI: C1970161
Disease: MECKEL SYNDROME, TYPE 4
MECKEL SYNDROME, TYPE 4 		1 0 1 3.3E-02 0 0
CUI: C2676788
Disease: JOUBERT SYNDROME 9 (disorder)
JOUBERT SYNDROME 9 (disorder) 		1 0 1 3.3E-02 0 0
CUI: C2676790
Disease: MECKEL SYNDROME, TYPE 6 (disorder)
MECKEL SYNDROME, TYPE 6 (disorder) 		1 0 1 3.3E-02 0 0
CUI: C3150796
Disease: NEPHRONOPHTHISIS 11
NEPHRONOPHTHISIS 11 		1 0 1 3.3E-02 0 0
CUI: C3275898
Disease: RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO
RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO 		1 0 1 3.3E-02 0 0
CUI: C3501830
Disease: Microcephaly, Primary Autosomal Recessive, 2
Microcephaly, Primary Autosomal Recessive, 2 		1 0 1 3.3E-02 0 0
CUI: C3554247
Disease: CARPENTER SYNDROME 2
CARPENTER SYNDROME 2 		1 0 1 3.3E-02 0 0
CUI: C3809087
Disease: CILIARY DYSKINESIA, PRIMARY, 21
CILIARY DYSKINESIA, PRIMARY, 21 		1 0 1 3.3E-02 0 0
CUI: C3809320
Disease: NEPHRONOPHTHISIS 16
NEPHRONOPHTHISIS 16 		1 0 1 3.3E-02 0 0
CUI: C3809548
Disease: CILIARY DYSKINESIA, PRIMARY, 23
CILIARY DYSKINESIA, PRIMARY, 23 		1 0 1 3.3E-02 0 0