Source: BEFREE ×
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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 6.4E-04
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 6.4E-04
CUI: C0268958
Disease: Acute orchitis
Acute orchitis 		0 1 0 0 1 6.4E-04
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 6.4E-04
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 6.4E-04
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 6.4E-04
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania 		0 1 0 0 1 6.4E-04
CUI: C0334328
Disease: Microfollicular adenoma
Microfollicular adenoma 		0 1 0 0 1 6.4E-04
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 1.3E-03
CUI: C0814144
Disease: endocrine system cancer
endocrine system cancer 		0 1 0 0 1 6.4E-04
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 2 1.3E-03
CUI: C0877781
Disease: Hemicrania
Hemicrania 		0 1 0 0 1 6.4E-04
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 6.4E-04
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 6.4E-04
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 6.4E-04
CUI: C4749271
Disease: Aleukemic mast cell leukemia
Aleukemic mast cell leukemia 		0 2 0 0 2 1.3E-03
CUI: C0265233
Disease: Cryptophthalmos syndrome
Cryptophthalmos syndrome 		6 0 1 9.8E-05 0 0
CUI: C0270851
Disease: Benign neonatal epilepsy
Benign neonatal epilepsy 		6 0 1 9.8E-05 0 0
CUI: C0585539
Disease: X-Linked Infantile Nystagmus
X-Linked Infantile Nystagmus 		6 0 1 9.8E-05 0 0
CUI: C2936406
Disease: alpha-Dystroglycanopathies
alpha-Dystroglycanopathies 		6 0 1 9.8E-05 0 0
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		5 2 1 9.8E-05 1 6.4E-04
CUI: C0403654
Disease: Bladder outflow obstruction
Bladder outflow obstruction 		5 0 1 9.8E-05 0 0
CUI: C0796225
Disease: Mental Retardation, X-Linked 19
Mental Retardation, X-Linked 19 		5 0 1 9.8E-05 0 0
CUI: C1456276
Disease: Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-like episodes (MELAS syndrome)
Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-like episodes (MELAS syndrome) 		5 0 1 9.8E-05 0 0
CUI: C1832525
Disease: Limb-girdle muscular dystrophy type 2F
Limb-girdle muscular dystrophy type 2F 		5 0 1 9.8E-05 0 0