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 1.2E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 1.2E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 2 0 0 1 1.2E-03
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 3 0 0 1 1.2E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 1.2E-03
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 1.2E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 2.3E-03
CUI: C0342759
Disease: Primary lactose intolerance
Primary lactose intolerance 		0 1 0 0 1 1.2E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 1.2E-03
CUI: C0814144
Disease: endocrine system cancer
endocrine system cancer 		0 1 0 0 1 1.2E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 2 2.3E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.2E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.2E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 1.2E-03
CUI: C0795949
Disease: Galloway Mowat syndrome
Galloway Mowat syndrome 		15 0 1 2.3E-04 0 0
CUI: C0342273
Disease: Transient neonatal diabetes mellitus
Transient neonatal diabetes mellitus 		12 0 1 2.3E-04 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		11 0 1 2.3E-04 0 0
CUI: C0342191
Disease: Familial dyshormonogenetic goiter
Familial dyshormonogenetic goiter 		11 0 1 2.3E-04 0 0
CUI: C0549225
Disease: Myasthenic Syndrome
Myasthenic Syndrome 		11 0 1 2.3E-04 0 0
CUI: C1955603
Disease: Deaf-Blind Disorders
Deaf-Blind Disorders 		11 0 1 2.3E-04 0 0
CUI: C0271986
Disease: delta beta^0^ Thalassemia
delta beta^0^ Thalassemia 		10 0 1 2.3E-04 0 0
CUI: C0342778
Disease: Ubiquinone dehydrogenase deficiency
Ubiquinone dehydrogenase deficiency 		10 0 1 2.3E-04 0 0
CUI: C0392485
Disease: Congenital diverticulum of pharynx
Congenital diverticulum of pharynx 		10 0 1 2.3E-04 0 0
CUI: C0432217
Disease: Wolcott-Rallison syndrome
Wolcott-Rallison syndrome 		10 0 1 2.3E-04 0 0
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome 		10 0 1 2.3E-04 0 0