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 5.2E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 5.4E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 5.4E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 5.4E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 5.3E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 5.4E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 2 1.1E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 5.4E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 1.6E-02
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet 		129 0 1 1.1E-03 0 0
CUI: C0576226
Disease: Short foot
Short foot 		116 0 1 1.1E-03 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 1.2E-03 0 0
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0 		87 0 1 1.2E-03 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0 		87 0 1 1.2E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.2E-03 0 0
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia 		77 0 1 1.2E-03 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 1.2E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 1.2E-03 0 0
CUI: C0376705
Disease: Viral Load result
Viral Load result 		65 0 1 1.2E-03 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		61 0 1 1.2E-03 0 0
CUI: C4022587
Disease: Fatigable weakness of respiratory muscles
Fatigable weakness of respiratory muscles 		60 0 1 1.2E-03 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 1.2E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		59 0 1 1.2E-03 0 0
CUI: C1859236
Disease: Prolonged neonatal jaundice
Prolonged neonatal jaundice 		59 0 1 1.2E-03 0 0
CUI: C3553450
Disease: Profound global developmental delay
Profound global developmental delay 		58 0 1 1.2E-03 0 0