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: C0332878
Disease: Congenital contracture
Congenital contracture 		31 0 1 6.6E-04 0 0
CUI: C0813217
Disease: Expressionless face
Expressionless face 		31 0 1 6.6E-04 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea 		31 0 1 6.6E-04 0 0
CUI: C1141890
Disease: Congenital long QT syndrome
Congenital long QT syndrome 		30 0 1 6.6E-04 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 1 6.6E-04 0 0
CUI: C1848201
Disease: Subcortical Band Heterotopia
Subcortical Band Heterotopia 		30 0 1 6.6E-04 0 0
CUI: C1855676
Disease: Aplasia/Hypoplasia of the cerebellar vermis
Aplasia/Hypoplasia of the cerebellar vermis 		30 0 1 6.6E-04 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 1 6.6E-04 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 1 6.6E-04 0 0
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy 		29 0 1 6.6E-04 0 0
CUI: C1321329
Disease: Slowed saccades
Slowed saccades 		29 0 1 6.6E-04 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 1 6.6E-04 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 1 6.6E-04 0 0
CUI: C4072872
Disease: obsolete Rod-cone dystrophy
obsolete Rod-cone dystrophy 		29 0 1 6.6E-04 0 0
CUI: C0344232
Disease: Blurred vision
Blurred vision 		28 0 1 6.6E-04 0 0
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness 		28 0 1 6.6E-04 0 0
CUI: C3158111
Disease: response to SSRI
response to SSRI 		28 0 1 6.6E-04 0 0
CUI: C3715208
Disease: AV Block First Degree by ECG Finding
AV Block First Degree by ECG Finding 		28 0 1 6.6E-04 0 0
CUI: C0878575
Disease: Peripheral demyelination
Peripheral demyelination 		27 0 1 6.6E-04 0 0
CUI: C4020730
Disease: Increased intramyocellular lipid droplets
Increased intramyocellular lipid droplets 		27 0 1 6.6E-04 0 0
CUI: C0085614
Disease: First degree atrioventricular block
First degree atrioventricular block 		26 0 1 6.6E-04 0 0
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia 		26 0 1 6.6E-04 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 1 6.6E-04 0 0
CUI: C0162275
Disease: Ketonuria
Ketonuria 		26 0 1 6.6E-04 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		26 0 1 6.6E-04 0 0