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: C0036904
Disease: Sexual desire disorder
Sexual desire disorder 		0 1 0 0 1 8.1E-03
CUI: C0233689
Disease: Delusion of infidelity
Delusion of infidelity 		0 1 0 0 1 8.1E-03
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 8.1E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 7.7E-03
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0 183 0 0 1 3.3E-03
CUI: C0549117
Disease: Frontal lobe syndrome
Frontal lobe syndrome 		0 3 0 0 1 7.9E-03
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		0 3 0 0 1 7.9E-03
CUI: C1855995
Disease: L-2-HYDROXYGLUTARIC ACIDURIA
L-2-HYDROXYGLUTARIC ACIDURIA 		0 16 0 0 1 7.2E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 8.1E-03
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome 		0 1 0 0 1 8.1E-03
CUI: C2242712
Disease: Hyper LDL cholesterolaemia
Hyper LDL cholesterolaemia 		0 19 0 0 1 7.0E-03
CUI: C2746066
Disease: Combined D-2- and L-2-hydroxyglutaric aciduria
Combined D-2- and L-2-hydroxyglutaric aciduria 		0 14 0 0 1 7.3E-03
CUI: C4551693
Disease: Wolfram Syndrome 1
Wolfram Syndrome 1 		0 36 0 0 1 6.3E-03
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		284 0 1 2.0E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		264 0 1 2.1E-03 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		223 0 1 2.3E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 0 1 2.4E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 2.5E-03 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		190 0 1 2.5E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 2.5E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 2.6E-03 0 0
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		176 0 1 2.6E-03 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		172 0 1 2.6E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.6E-03 0 0
CUI: C1837260
Disease: Prominent forehead
Prominent forehead 		159 0 1 2.7E-03 0 0