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: C0033923
Disease: Psychomotor Performance
Psychomotor Performance 		0 1 0 0 1 3.7E-04
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.7E-04
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 3.7E-04
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.7E-04
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 7.5E-04
CUI: C0342759
Disease: Primary lactose intolerance
Primary lactose intolerance 		0 1 0 0 1 3.7E-04
CUI: C0373601
Disease: Dihydrotestosterone Assay
Dihydrotestosterone Assay 		0 2 0 0 1 3.7E-04
CUI: C0696098
Disease: Blood thyroid stimulating hormone analysis
Blood thyroid stimulating hormone analysis 		0 7 0 0 1 3.7E-04
CUI: C0696105
Disease: Beta carotene measurement
Beta carotene measurement 		0 2 0 0 1 3.7E-04
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 3.7E-04
CUI: C1834750
Disease: CORONARY ARTERY DISEASE, MODIFIER OF
CORONARY ARTERY DISEASE, MODIFIER OF 		0 1 0 0 1 3.7E-04
CUI: C1834751
Disease: CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV 		0 1 0 0 1 3.7E-04
CUI: C1862591
Disease: CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO 		0 1 0 0 1 3.7E-04
CUI: C1868512
Disease: Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 		0 2 0 0 1 3.7E-04
CUI: C1997262
Disease: Hypothyroidism in pregnancy
Hypothyroidism in pregnancy 		0 1 0 0 1 3.7E-04
CUI: C2242456
Disease: thyroid function
thyroid function 		0 60 0 0 1 3.7E-04
CUI: C2699063
Disease: Resistin Measurement
Resistin Measurement 		0 6 0 0 1 3.7E-04
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 3.7E-04
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.7E-04
CUI: C4016190
Disease: DELTA-PLUS-THALASSEMIA
DELTA-PLUS-THALASSEMIA 		0 1 0 0 1 3.7E-04
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 3.7E-04
CUI: C4016417
Disease: VASCULAR DEMENTIA, SUSCEPTIBILITY TO
VASCULAR DEMENTIA, SUSCEPTIBILITY TO 		0 1 0 0 1 3.7E-04
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 3.7E-04
CUI: C0000727
Disease: Abdomen, Acute
Abdomen, Acute 		2 0 1 3.2E-04 0 0
CUI: C0001079
Disease: Achondrogenesis
Achondrogenesis 		4 0 1 3.2E-04 0 0