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 4.2E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 6.2E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 2 0.11
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
Hemiplegic migraine, familial type 1 		0 37 0 0 1 1.9E-02
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0 14 0 0 1 3.4E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 5.6E-02
CUI: C3825462
Disease: Diabetes in youth
Diabetes in youth 		0 2 0 0 1 5.9E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 6.2E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 0.12
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.0E-03 0 0
CUI: C0038580
Disease: Substance Dependence
Substance Dependence 		156 0 1 2.0E-03 0 0
CUI: C0013222
Disease: Drug Use Disorders
Drug Use Disorders 		121 0 1 2.2E-03 0 0
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		104 0 1 2.2E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 2.3E-03 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers 		92 0 1 2.3E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		90 0 1 2.3E-03 0 0
CUI: C1853241
Disease: Flat face
Flat face 		83 0 1 2.3E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 2.4E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 2.4E-03 0 0
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		80 0 1 2.4E-03 0 0
CUI: C0241726
Disease: Delayed ability to walk
Delayed ability to walk 		77 0 1 2.4E-03 0 0
CUI: C0012569
Disease: Diplopia
Diplopia 		75 0 1 2.4E-03 0 0
CUI: C0202202
Disease: Protein measurement
Protein measurement 		75 0 1 2.4E-03 0 0
CUI: C1527366
Disease: Salaam Seizures
Salaam Seizures 		75 0 1 2.4E-03 0 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		75 0 1 2.4E-03 0 0