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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.6E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 1.6E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 1.5E-02
CUI: C2697788
Disease: Interleukin 8 Measurement
Interleukin 8 Measurement 		0 5 0 0 1 1.5E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.6E-02
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		82 0 1 7.9E-04 0 0
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia 		77 0 1 8.0E-04 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 8.0E-04 0 0
CUI: C0406208
Disease: Suntan
Suntan 		53 0 1 8.1E-04 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 1 8.2E-04 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		45 0 1 8.2E-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 8.2E-04 0 0
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		41 0 1 8.2E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 8.2E-04 0 0
CUI: C2677650
Disease: Decreased activity of mitochondrial complex I
Decreased activity of mitochondrial complex I 		41 0 1 8.2E-04 0 0
CUI: C4021741
Disease: Abnormal cortical bone morphology
Abnormal cortical bone morphology 		41 0 1 8.2E-04 0 0
CUI: C4023687
Disease: EEG with multifocal slow activity
EEG with multifocal slow activity 		41 0 1 8.2E-04 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 8.2E-04 0 0
CUI: C4024780
Disease: Almond-shaped palpebral fissure
Almond-shaped palpebral fissure 		40 0 1 8.2E-04 0 0
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block 		39 0 1 8.2E-04 0 0
CUI: C0431350
Disease: Primary microcephaly
Primary microcephaly 		39 0 1 8.2E-04 0 0
CUI: C2749675
Disease: Cortical gyral simplification
Cortical gyral simplification 		39 0 1 8.2E-04 0 0
CUI: C4023342
Disease: Gastrostomy tube feeding in infancy
Gastrostomy tube feeding in infancy 		38 0 1 8.2E-04 0 0
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		37 0 1 8.2E-04 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy 		37 0 1 8.2E-04 0 0