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: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0 350 0 0 2 5.4E-03
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction
0 2 0 0 1 4.5E-02
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
0 8 0 0 1 3.6E-02
CUI: C0003467
Disease: Anxiety
Anxiety
0 169 0 0 1 5.3E-03
CUI: C0003492
Disease: Aortic coarctation
Aortic coarctation
0 3 0 0 1 4.3E-02
CUI: C0003635
Disease: Apraxias
Apraxias
0 7 0 0 1 3.7E-02
CUI: C0004134
Disease: Ataxia
Ataxia
0 17 0 0 1 2.7E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0 181 0 0 1 5.0E-03
CUI: C0004604
Disease: Back Pain
Back Pain
0 7 0 0 1 3.7E-02
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
0 49 0 0 1 1.4E-02
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0 455 0 0 1 2.1E-03
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
0 58 0 0 1 1.3E-02
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
0 35 0 0 6 0.12
Congenital ocular coloboma (disorder)
0 12 0 0 2 6.5E-02
CUI: C0009806
Disease: Constipation
Constipation
0 49 0 0 1 1.4E-02
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis
0 33 0 0 1 1.9E-02
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism
0 9 0 0 1 3.4E-02
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
0 48 0 0 1 1.5E-02
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0 39 0 0 2 3.4E-02
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle
0 5 0 0 1 4.0E-02
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus
0 25 0 0 2 4.5E-02
CUI: C0013362
Disease: Dysarthria
Dysarthria
0 42 0 0 1 1.6E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 8 0 0 1 3.6E-02
CUI: C0014877
Disease: Esotropia
Esotropia
0 39 0 0 3 5.3E-02
CUI: C0015310
Disease: Exotropia
Exotropia
0 21 0 0 1 2.4E-02