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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.4E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.4E-03
CUI: C0036904
Disease: Sexual desire disorder
Sexual desire disorder 		0 1 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 1 1.4E-03
CUI: C0730278
Disease: Severe nonproliferative diabetic retinopathy
Severe nonproliferative diabetic retinopathy 		0 3 0 0 1 1.4E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 1.4E-03
CUI: C3178803
Disease: Social Anhedonia
Social Anhedonia 		0 4 0 0 1 1.4E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.4E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.4E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 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: C1857679
Disease: Sloping forehead
Sloping forehead 		149 0 1 6.9E-04 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 7.2E-04 0 0
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia 		77 0 1 7.2E-04 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 7.2E-04 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 7.3E-04 0 0
CUI: C1862095
Disease: Bilateral single transverse palmar creases
Bilateral single transverse palmar creases 		65 0 1 7.3E-04 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum 		63 0 1 7.3E-04 0 0
CUI: C0231687
Disease: Spastic gait
Spastic gait 		62 0 1 7.3E-04 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		61 0 1 7.3E-04 0 0
CUI: C1854418
Disease: Biparietal narrowing
Biparietal narrowing 		60 0 1 7.3E-04 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		59 0 1 7.3E-04 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers 		59 0 1 7.3E-04 0 0
CUI: C3553450
Disease: Profound global developmental delay
Profound global developmental delay 		58 0 1 7.3E-04 0 0