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 2.0E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 2.0E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 2.0E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 2.0E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 2.0E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 4.0E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 2.0E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 2.0E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 2.0E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.0E-03
CUI: C4722327
Disease: PROSTATE CANCER, HEREDITARY, 1
PROSTATE CANCER, HEREDITARY, 1 		0 1 0 0 1 2.0E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 6.0E-03
CUI: C3468114
Disease: Juvenile amyotrophic lateral sclerosis
Juvenile amyotrophic lateral sclerosis 		20 0 1 2.7E-04 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		19 0 1 2.7E-04 0 0
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy 		18 0 1 2.7E-04 0 0
CUI: C0029294
Disease: Orofaciodigital Syndromes
Orofaciodigital Syndromes 		17 0 1 2.7E-04 0 0
CUI: C1858712
Disease: Spastic paraplegia 10, autosomal dominant
Spastic paraplegia 10, autosomal dominant 		16 0 1 2.7E-04 0 0
CUI: C1859722
Disease: Arthrogryposis, renal dysfunction, and cholestasis 1
Arthrogryposis, renal dysfunction, and cholestasis 1 		16 0 1 2.7E-04 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		16 0 1 2.7E-04 0 0
CUI: C0036996
Disease: Short Rib-Polydactyly Syndrome
Short Rib-Polydactyly Syndrome 		14 0 1 2.7E-04 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 1 2.7E-04 0 0
CUI: C0154823
Disease: Retinal defect
Retinal defect 		13 0 1 2.7E-04 0 0
CUI: C0457133
Disease: Muscle eye brain disease
Muscle eye brain disease 		13 0 1 2.7E-04 0 0
CUI: C0271985
Disease: Delta-Beta Thalassemia
Delta-Beta Thalassemia 		12 0 1 2.7E-04 0 0
CUI: C4087273
Disease: C3 glomerulopathy
C3 glomerulopathy 		12 0 1 2.7E-04 0 0