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: C0236048
Disease: Polyposis, Gastric
Polyposis, Gastric 		0 4 0 0 1 3.4E-03
CUI: C0857262
Disease: Bi-ventricular failure
Bi-ventricular failure 		0 1 0 0 1 3.4E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 3.4E-03
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		67 0 1 1.0E-03 0 0
CUI: C0376705
Disease: Viral Load result
Viral Load result 		65 0 1 1.0E-03 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 1.0E-03 0 0
CUI: C4021219
Disease: Multifocal epileptiform discharges
Multifocal epileptiform discharges 		52 0 1 1.0E-03 0 0
CUI: C0345354
Disease: Radial polydactyly
Radial polydactyly 		51 0 1 1.0E-03 0 0
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		51 0 1 1.0E-03 0 0
CUI: C0238395
Disease: Male Pseudohermaphroditism
Male Pseudohermaphroditism 		50 0 1 1.0E-03 0 0
CUI: C0265677
Disease: Congenital hemivertebra
Congenital hemivertebra 		49 0 1 1.0E-03 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 1.0E-03 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 1.0E-03 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 1.0E-03 0 0
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		41 0 1 1.0E-03 0 0
CUI: C0581354
Disease: Recurrent sinusitis
Recurrent sinusitis 		41 0 1 1.0E-03 0 0
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		41 0 1 1.0E-03 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 1 1.0E-03 0 0
CUI: C4023687
Disease: EEG with multifocal slow activity
EEG with multifocal slow activity 		41 0 1 1.0E-03 0 0
CUI: C1288283
Disease: Atrophoderma maculatum
Atrophoderma maculatum 		39 0 1 1.0E-03 0 0
CUI: C2749675
Disease: Cortical gyral simplification
Cortical gyral simplification 		39 0 1 1.0E-03 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 1.0E-03 0 0
CUI: C0239399
Disease: Short extremities
Short extremities 		38 0 1 1.0E-03 0 0
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		37 0 1 1.0E-03 0 0
CUI: C0010093
Disease: Corpus Luteum Cyst
Corpus Luteum Cyst 		36 0 1 1.0E-03 0 0