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: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		45 0 1 8.4E-04 0 0
CUI: C2931498
Disease: Mental Retardation, X-Linked 1
Mental Retardation, X-Linked 1 		45 0 1 8.4E-04 0 0
CUI: C2076600
Disease: Influenza due to Influenza A virus subtype H1N1
Influenza due to Influenza A virus subtype H1N1 		44 0 1 8.4E-04 0 0
CUI: C4551906
Disease: Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		43 0 1 8.4E-04 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 8.4E-04 0 0
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		41 0 1 8.5E-04 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 1 8.5E-04 0 0
CUI: C0581354
Disease: Recurrent sinusitis
Recurrent sinusitis 		41 0 1 8.5E-04 0 0
CUI: C1859470
Disease: Large basal ganglia
Large basal ganglia 		41 0 1 8.5E-04 0 0
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		41 0 1 8.5E-04 0 0
CUI: C0003126
Disease: Anosmia
Anosmia 		40 0 1 8.5E-04 0 0
CUI: C1276035
Disease: Pena-Shokeir syndrome type I
Pena-Shokeir syndrome type I 		40 0 1 8.5E-04 0 0
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block 		39 0 1 8.5E-04 0 0
CUI: C0266174
Disease: Duodenal atresia
Duodenal atresia 		39 0 1 8.5E-04 0 0
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		39 0 1 8.5E-04 0 0
CUI: C1847515
Disease: Paroxysmal involuntary eye movements
Paroxysmal involuntary eye movements 		39 0 1 8.5E-04 0 0
CUI: C3489393
Disease: Hiatal Hernia
Hiatal Hernia 		39 0 1 8.5E-04 0 0
CUI: C4021546
Disease: Abnormal mitochondria in muscle tissue
Abnormal mitochondria in muscle tissue 		39 0 1 8.5E-04 0 0
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		39 0 1 8.5E-04 0 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		38 0 1 8.5E-04 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 1 8.5E-04 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		37 0 1 8.5E-04 0 0
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		37 0 1 8.5E-04 0 0
CUI: C0238397
Disease: Pulmonary artery stenosis
Pulmonary artery stenosis 		36 0 1 8.5E-04 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly 		35 0 1 8.5E-04 0 0