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: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		0 11 0 0 1 7.6E-03
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 1 8.2E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 8.2E-03
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 2.5E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 2.5E-03 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal 		227 0 1 2.6E-03 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia 		226 0 1 2.6E-03 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 0 1 2.6E-03 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		217 0 1 2.6E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 2.6E-03 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		213 0 1 2.7E-03 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 0 1 2.7E-03 0 0
CUI: C0152421
Disease: Macrotia
Macrotia 		188 0 1 2.8E-03 0 0
CUI: C1839839
Disease: MAJOR AFFECTIVE DISORDER 2
MAJOR AFFECTIVE DISORDER 2 		185 0 1 2.9E-03 0 0
CUI: C1836047
Disease: Long face
Long face 		182 0 1 2.9E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 2.9E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 2.9E-03 0 0
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		176 0 1 2.9E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 1 3.0E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 3.0E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 3.0E-03 0 0
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders 		167 0 1 3.0E-03 0 0
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive 		166 0 1 3.0E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 3.0E-03 0 0
CUI: C1852197
Disease: MAJOR AFFECTIVE DISORDER 1
MAJOR AFFECTIVE DISORDER 1 		161 0 1 3.1E-03 0 0