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: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome 		0 3 0 0 1 1.6E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.4E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.6E-02
CUI: C0234253
Disease: Rest pain
Rest pain 		0 1 0 0 1 1.6E-02
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 1.6E-02
CUI: C0266427
Disease: Testicular regression syndrome
Testicular regression syndrome 		0 3 0 0 1 1.6E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.5E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 2 3.1E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 1.6E-02
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 1.6E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.6E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.6E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.6E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 1.6E-02
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 1.6E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 1.4E-02
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 2.2E-03 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		172 0 1 2.9E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.9E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 2.9E-03 0 0
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		168 0 1 2.9E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 2.9E-03 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 0 1 2.9E-03 0 0
CUI: C3468561
Disease: familial atrial fibrillation
familial atrial fibrillation 		157 0 1 3.0E-03 0 0
CUI: C2585653
Disease: Persistent atrial fibrillation
Persistent atrial fibrillation 		156 0 1 3.0E-03 0 0