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 2.2E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.6E-02
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 2.6E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 2.3E-02
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 2.6E-02
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 2.6E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 2.5E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.6E-02
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 2.6E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 7.9E-02
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 2.1E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 2.1E-03 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 0 1 2.2E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 0 1 2.2E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 2.3E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 2.3E-03 0 0
CUI: C1836047
Disease: Long face
Long face 		182 0 1 2.4E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 2.4E-03 0 0
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		171 0 1 2.4E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 2.4E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.5E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation 		160 0 1 2.5E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		156 0 1 2.5E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency 		148 0 1 2.6E-03 0 0
CUI: C1858430
Disease: Death in infancy
Death in infancy 		146 0 1 2.6E-03 0 0