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 9.9E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.1E-02
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 1.1E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.0E-02
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.1E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 3 3.2E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 1.1E-02
CUI: C2676507
Disease: Inflammatory Bowel Disease 21
Inflammatory Bowel Disease 21 		0 1 0 0 1 1.1E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.1E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.1E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 3.2E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 1 9.2E-04 0 0
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		427 0 1 1.5E-03 0 0
CUI: C0037369
Disease: Smoking
Smoking 		391 0 1 1.6E-03 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		291 0 1 1.9E-03 0 0
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		249 0 1 2.1E-03 0 0
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 2.2E-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: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		192 0 1 2.4E-03 0 0
CUI: C0037822
Disease: Speech Disorders
Speech Disorders 		183 0 1 2.4E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 2.4E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 2.4E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 2.5E-03 0 0