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: C0014761
Disease: Erythroblastosis, Fetal
Erythroblastosis, Fetal 		15 0 1 3.3E-04 0 0
CUI: C0685838
Disease: Gonadal dysgenesis XX type deafness
Gonadal dysgenesis XX type deafness 		14 0 1 3.3E-04 0 0
CUI: C1839615
Disease: X-linked myopathy with excessive autophagy
X-linked myopathy with excessive autophagy 		14 0 1 3.3E-04 0 0
CUI: C4054085
Disease: Refractory Childhood Acute Lymphoblastic Leukemia
Refractory Childhood Acute Lymphoblastic Leukemia 		13 0 1 3.3E-04 0 0
CUI: C0020599
Disease: Hypocalciuria
Hypocalciuria 		12 0 1 3.3E-04 0 0
CUI: C0024106
Disease: Lumpy Skin Disease
Lumpy Skin Disease 		12 0 1 3.3E-04 0 0
CUI: C0268425
Disease: Alstrom Syndrome
Alstrom Syndrome 		12 0 1 3.3E-04 0 0
CUI: C0339002
Disease: Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type
Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type 		12 0 1 3.3E-04 0 0
CUI: C0857116
Disease: Gross obesity
Gross obesity 		12 0 1 3.3E-04 0 0
CUI: C2936694
Disease: Swyer Syndrome
Swyer Syndrome 		12 0 1 3.3E-04 0 0
CUI: C3714580
Disease: Hypokalemic periodic paralysis type 1
Hypokalemic periodic paralysis type 1 		12 0 1 3.3E-04 0 0
CUI: C0011430
Disease: Dentin Dysplasia
Dentin Dysplasia 		11 0 1 3.3E-04 0 0
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2 		11 0 1 3.3E-04 0 0
CUI: C0549225
Disease: Myasthenic Syndrome
Myasthenic Syndrome 		11 0 1 3.3E-04 0 0
CUI: C0701818
Disease: Choledocholithiasis
Choledocholithiasis 		11 0 1 3.3E-04 0 0
CUI: C1847640
Disease: KUFOR-RAKEB SYNDROME
KUFOR-RAKEB SYNDROME 		11 0 1 3.3E-04 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		11 0 1 3.3E-04 0 0
CUI: C4288302
Disease: Refractory Adult Acute Lymphoblastic Leukemia
Refractory Adult Acute Lymphoblastic Leukemia 		11 0 1 3.3E-04 0 0
CUI: C0013903
Disease: Ellis-Van Creveld Syndrome
Ellis-Van Creveld Syndrome 		10 0 1 3.3E-04 0 0
CUI: C0149841
Disease: Benign recurrent intrahepatic cholestasis
Benign recurrent intrahepatic cholestasis 		10 0 1 3.3E-04 0 0
CUI: C0234376
Disease: Action Tremor
Action Tremor 		10 0 1 3.3E-04 0 0
CUI: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome 		10 0 1 3.3E-04 0 0
CUI: C0342778
Disease: Ubiquinone dehydrogenase deficiency
Ubiquinone dehydrogenase deficiency 		10 0 1 3.3E-04 0 0
CUI: C0344432
Disease: Ventricular tachycardia, polymorphic
Ventricular tachycardia, polymorphic 		10 0 1 3.3E-04 0 0
CUI: C0349653
Disease: Congenital disorder of glycosylation type 1A
Congenital disorder of glycosylation type 1A 		10 0 1 3.3E-04 0 0