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: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		237 0 1 4.2E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 5.7E-03 0 0
CUI: C0003492
Disease: Aortic coarctation
Aortic coarctation 		64 0 1 1.6E-02 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		99 0 1 1.0E-02 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		244 0 1 4.1E-03 0 0
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis 		96 0 1 1.0E-02 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		574 0 1 1.7E-03 0 0
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate 		16 0 1 6.2E-02 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: C0009806
Disease: Constipation
Constipation 		289 0 1 3.5E-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: C0013132
Disease: Drooling
Drooling 		94 0 1 1.1E-02 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism 		1039 0 1 9.6E-04 0 0
CUI: C0015469
Disease: Facial paralysis
Facial paralysis 		165 0 1 6.1E-03 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot 		282 0 1 3.5E-03 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		259 0 1 3.9E-03 0 0
CUI: C0016873
Disease: Fused Teeth
Fused Teeth 		4 0 1 0.25 0 0
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		281 0 1 3.6E-03 0 0
CUI: C0018524
Disease: Hallucinations
Hallucinations 		126 0 1 7.9E-03 0 0
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		622 0 1 1.6E-03 0 0
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects 		61 0 1 1.6E-02 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		250 0 1 4.0E-03 0 0