Source: INFERRED ×
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: C0002170
Disease: Alopecia
Alopecia 		261 0 1 3.8E-03 0 0
CUI: C0003126
Disease: Anosmia
Anosmia 		39 0 1 2.6E-02 0 0
CUI: C0003467
Disease: Anxiety
Anxiety 		336 0 1 3.0E-03 0 0
CUI: C0003492
Disease: Aortic coarctation
Aortic coarctation 		64 0 1 1.6E-02 0 0
CUI: C0003507
Disease: Aortic Valve Stenosis
Aortic Valve Stenosis 		47 0 1 2.1E-02 0 0
CUI: C0003537
Disease: Aphasia
Aphasia 		56 0 1 1.8E-02 0 0
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation 		43 0 1 2.3E-02 0 0
CUI: C0004096
Disease: Asthma
Asthma 		446 0 1 2.2E-03 0 0
CUI: C0004114
Disease: Astrocytoma
Astrocytoma 		21 0 1 4.8E-02 0 0
CUI: C0004134
Disease: Ataxia
Ataxia 		609 0 1 1.6E-03 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		244 0 1 4.1E-03 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		574 0 1 1.7E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height 		1903 0 1 5.3E-04 0 0
CUI: C0005937
Disease: Bone Cysts
Bone Cysts 		25 0 1 4.0E-02 0 0
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		165 0 1 6.1E-03 0 0
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia 		100 0 1 1.0E-02 0 0
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		165 0 1 6.1E-03 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		446 0 1 2.2E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		80 0 1 1.3E-02 0 0
CUI: C0009806
Disease: Constipation
Constipation 		289 0 1 3.5E-03 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		107 0 1 9.3E-03 0 0
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		107 0 1 9.3E-03 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		596 0 1 1.7E-03 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		111 0 1 9.0E-03 0 0
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		304 0 1 3.3E-03 0 0