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: C0033923
Disease: Psychomotor Performance
Psychomotor Performance 		0 1 0 0 1 1.4E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.4E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 1.4E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 1.4E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 2.8E-03
CUI: C0678189
Disease: Hyperlipidemia, group A
Hyperlipidemia, group A 		0 1 0 0 1 1.4E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 1.4E-03
CUI: C1997262
Disease: Hypothyroidism in pregnancy
Hypothyroidism in pregnancy 		0 1 0 0 1 1.4E-03
CUI: C2242456
Disease: thyroid function
thyroid function 		0 60 0 0 1 1.3E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 2 2.8E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.4E-03
CUI: C3888516
Disease: CYP1A2 polymorphism
CYP1A2 polymorphism 		0 2 0 0 1 1.4E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 1.4E-03
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 5.5E-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 5.6E-04 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 5.6E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 5.6E-04 0 0
CUI: C2677650
Disease: Decreased activity of mitochondrial complex I
Decreased activity of mitochondrial complex I 		41 0 1 5.6E-04 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 5.6E-04 0 0
CUI: C2749675
Disease: Cortical gyral simplification
Cortical gyral simplification 		39 0 1 5.6E-04 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		37 0 1 5.6E-04 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy 		37 0 1 5.6E-04 0 0
CUI: C0744356
Disease: Abnormality of the genital system
Abnormality of the genital system 		36 0 1 5.6E-04 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		36 0 1 5.6E-04 0 0
CUI: C0078982
Disease: Arhinencephaly
Arhinencephaly 		35 0 1 5.6E-04 0 0