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 1.1E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.2E-02
CUI: C0149955
Disease: Annular pancreas
Annular pancreas 		0 1 0 0 1 1.2E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 1.2E-02
CUI: C0341472
Disease: Obstructive chronic pancreatitis
Obstructive chronic pancreatitis 		0 1 0 0 1 1.2E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 1.2E-02
CUI: C1969419
Disease: PANCREATITIS, CHRONIC, SUSCEPTIBILITY TO
PANCREATITIS, CHRONIC, SUSCEPTIBILITY TO 		0 3 0 0 1 1.2E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.2E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.2E-02
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 1 1.2E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 1.2E-03 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 1.2E-03 0 0
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 0 1 1.2E-03 0 0
CUI: C0040433
Disease: Tooth Crowding
Tooth Crowding 		82 0 1 1.2E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 1.2E-03 0 0
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		82 0 1 1.2E-03 0 0
CUI: C0241726
Disease: Delayed ability to walk
Delayed ability to walk 		77 0 1 1.2E-03 0 0
CUI: C1301937
Disease: Talipes
Talipes 		74 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: C0339789
Disease: Congenital deafness
Congenital deafness 		72 0 1 1.2E-03 0 0
CUI: C4025819
Disease: Abnormality of the hypothalamus-pituitary axis
Abnormality of the hypothalamus-pituitary axis 		70 0 1 1.2E-03 0 0
CUI: C0423867
Disease: Fine hair
Fine hair 		69 0 1 1.2E-03 0 0
CUI: C1850456
Disease: Progressive microcephaly
Progressive microcephaly 		67 0 1 1.2E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 1 1.2E-03 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly 		62 0 1 1.2E-03 0 0