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: C0042818
Disease: Visual discomfort
Visual discomfort 		1 0 1 9.6E-03 0 0
CUI: C0149877
Disease: Hypoglycemic encephalopathy
Hypoglycemic encephalopathy 		1 0 1 9.6E-03 0 0
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 9.6E-03 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 9.6E-03 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 9.6E-03 0 0
CUI: C0234174
Disease: Sucking reflex
Sucking reflex 		1 0 1 9.6E-03 0 0
CUI: C0234966
Disease: Astasia
Astasia 		1 0 1 9.6E-03 0 0
CUI: C0236701
Disease: Cocaine-induced mood disorder
Cocaine-induced mood disorder 		1 0 1 9.6E-03 0 0
CUI: C0236828
Disease: Articulation Disorders, Developmental
Articulation Disorders, Developmental 		1 0 1 9.6E-03 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 9.6E-03 0 0
CUI: C0264954
Disease: Arteriovascular degeneration
Arteriovascular degeneration 		1 0 1 9.6E-03 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 9.6E-03 0 0
CUI: C0265605
Disease: Congenital anomaly of finger
Congenital anomaly of finger 		1 0 1 9.6E-03 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 9.6E-03 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus 		1 0 1 9.6E-03 0 0
CUI: C0268262
Disease: Metachromatic Leukodystrophy due to Saposin B Deficiency
Metachromatic Leukodystrophy due to Saposin B Deficiency 		1 7 1 9.6E-03 1 7.3E-03
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I 		1 0 1 9.6E-03 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II 		1 0 1 9.6E-03 0 0
CUI: C0342376
Disease: Panhypopituitarism - X-linked
Panhypopituitarism - X-linked 		1 0 1 9.6E-03 0 0
CUI: C0342844
Disease: Disorder of glycoprotein metabolism
Disorder of glycoprotein metabolism 		1 0 1 9.6E-03 0 0
CUI: C0344487
Disease: Lateral meningocele
Lateral meningocele 		1 0 1 9.6E-03 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 9.6E-03 0 0
CUI: C0424000
Disease: Feeling suicidal (finding)
Feeling suicidal (finding) 		1 0 1 9.6E-03 0 0
CUI: C0429803
Disease: Bladder trabeculation
Bladder trabeculation 		1 0 1 9.6E-03 0 0
CUI: C0431501
Disease: Bilateral arterial duct
Bilateral arterial duct 		1 0 1 9.6E-03 0 0