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: C0015458
Disease: Facial Hemiatrophy
Facial Hemiatrophy 		0 4 0 0 1 2.3E-03
CUI: C0033923
Disease: Psychomotor Performance
Psychomotor Performance 		0 1 0 0 1 2.3E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.3E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 2.3E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 2.2E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 2.3E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 4.5E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 2.3E-03
CUI: C0730278
Disease: Severe nonproliferative diabetic retinopathy
Severe nonproliferative diabetic retinopathy 		0 3 0 0 1 2.3E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 2.3E-03
CUI: C0752138
Disease: Intracranial Arterial Diseases
Intracranial Arterial Diseases 		0 1 0 0 1 2.3E-03
CUI: C1401162
Disease: Carbohydrate intolerance
Carbohydrate intolerance 		0 1 0 0 1 2.3E-03
CUI: C1852324
Disease: ALDOSTERONE TO RENIN RATIO, INCREASED
ALDOSTERONE TO RENIN RATIO, INCREASED 		0 1 0 0 1 2.3E-03
CUI: C2699063
Disease: Resistin Measurement
Resistin Measurement 		0 6 0 0 2 4.5E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 2 4.5E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.3E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 2.3E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 4.5E-03
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion 		79 0 1 7.4E-04 0 0
CUI: C0241726
Disease: Delayed ability to walk
Delayed ability to walk 		77 0 1 7.4E-04 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		61 0 1 7.5E-04 0 0
CUI: C4021219
Disease: Multifocal epileptiform discharges
Multifocal epileptiform discharges 		52 0 1 7.5E-04 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 7.5E-04 0 0
CUI: C1849488
Disease: Increased serum pyruvate
Increased serum pyruvate 		45 0 1 7.5E-04 0 0
CUI: C0234860
Disease: Weak cry
Weak cry 		42 0 1 7.6E-04 0 0