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 8.4E-04
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 8.4E-04
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 8.4E-04
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 8.4E-04
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 8.4E-04
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 1.7E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 8.4E-04
CUI: C1275149
Disease: Multiple skin tags
Multiple skin tags 		0 1 0 0 1 8.4E-04
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 8.4E-04
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 8.4E-04
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 8.4E-04
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 8.4E-04
CUI: C4722327
Disease: PROSTATE CANCER, HEREDITARY, 1
PROSTATE CANCER, HEREDITARY, 1 		0 1 0 0 1 8.4E-04
CUI: C0457133
Disease: Muscle eye brain disease
Muscle eye brain disease 		13 0 1 2.0E-04 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		11 0 1 2.0E-04 0 0
CUI: C0332915
Disease: Congenital failure of fusion
Congenital failure of fusion 		11 0 1 2.0E-04 0 0
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		11 0 1 2.0E-04 0 0
CUI: C0342778
Disease: Ubiquinone dehydrogenase deficiency
Ubiquinone dehydrogenase deficiency 		10 0 1 2.0E-04 0 0
CUI: C0543918
Disease: SCHIZOPHRENIA 10
SCHIZOPHRENIA 10 		10 0 1 2.0E-04 0 0
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 0 1 2.0E-04 0 0
CUI: C0752202
Disease: Childhood Onset Dystonias
Childhood Onset Dystonias 		9 0 1 2.0E-04 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 1 2.0E-04 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 1 2.0E-04 0 0
CUI: C4317339
Disease: Juvenile Absence Epilepsy
Juvenile Absence Epilepsy 		9 0 1 2.0E-04 0 0
CUI: C0016510
Disease: Foot Diseases
Foot Diseases 		8 0 1 2.0E-04 0 0