Source: BEFREE ×
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: C0266617
Disease: Congenital anomaly of face
Congenital anomaly of face 		106 0 1 2.7E-03 0 0
CUI: C0282577
Disease: Congenital Disorders of Glycosylation
Congenital Disorders of Glycosylation 		100 0 1 2.7E-03 0 0
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		96 0 1 2.7E-03 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 0 1 2.8E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		81 0 1 2.9E-03 0 0
CUI: C1384514
Disease: Conn Syndrome
Conn Syndrome 		81 0 1 2.9E-03 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		80 0 1 2.9E-03 0 0
CUI: C1868938
Disease: End stage cardiac failure
End stage cardiac failure 		76 0 1 2.9E-03 0 0
CUI: C0013720
Disease: Ehlers-Danlos Syndrome
Ehlers-Danlos Syndrome 		75 0 1 2.9E-03 0 0
CUI: C0087169
Disease: Withdrawal Symptoms
Withdrawal Symptoms 		75 0 1 2.9E-03 0 0
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction 		75 0 1 2.9E-03 0 0
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular 		74 0 1 2.9E-03 0 0
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		73 0 1 2.9E-03 0 0
CUI: C0339510
Disease: Vitelliform Macular Dystrophy
Vitelliform Macular Dystrophy 		73 0 1 2.9E-03 0 0
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		72 0 1 2.9E-03 0 0
CUI: C0027709
Disease: Nephrocalcinosis
Nephrocalcinosis 		72 0 1 2.9E-03 0 0
CUI: C0234119
Disease: Neuromuscular inhibition
Neuromuscular inhibition 		72 0 1 2.9E-03 0 0
CUI: C0339789
Disease: Congenital deafness
Congenital deafness 		72 0 1 2.9E-03 0 0
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		70 0 1 2.9E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		68 0 1 3.0E-03 0 0
CUI: C0220994
Disease: Hyperammonemia
Hyperammonemia 		67 0 1 3.0E-03 0 0
CUI: C1285498
Disease: Vegetation
Vegetation 		67 0 1 3.0E-03 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		66 0 1 3.0E-03 0 0
CUI: C0424101
Disease: Inattention
Inattention 		66 0 1 3.0E-03 0 0
CUI: C0079504
Disease: Hermanski-Pudlak Syndrome
Hermanski-Pudlak Syndrome 		63 0 1 3.0E-03 0 0