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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic 		0 1 0 0 1 6.2E-03
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 23 0 0 1 5.4E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 6.1E-03
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement 		0 8 0 0 1 5.9E-03
CUI: C1299432
Disease: Multi vessel coronary artery disease
Multi vessel coronary artery disease 		0 1 0 0 1 6.2E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 6.2E-03
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses 		45 0 1 1.1E-03 0 0
CUI: C0015393
Disease: Eye Abnormalities
Eye Abnormalities 		38 0 1 1.2E-03 0 0
CUI: C0036875
Disease: Disorders of Sex Development
Disorders of Sex Development 		34 0 1 1.2E-03 0 0
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		33 0 1 1.2E-03 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome 		31 0 1 1.2E-03 0 0
CUI: C0019269
Disease: Hermaphroditism
Hermaphroditism 		29 0 1 1.2E-03 0 0
CUI: C0020302
Disease: Hydrophthalmos
Hydrophthalmos 		29 0 1 1.2E-03 0 0
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development 		29 0 1 1.2E-03 0 0
CUI: C0018051
Disease: Gonadal Dysgenesis
Gonadal Dysgenesis 		27 0 1 1.2E-03 0 0
CUI: C0026705
Disease: Mucopolysaccharidosis II
Mucopolysaccharidosis II 		26 0 1 1.2E-03 0 0
CUI: C0338430
Disease: Limbic Encephalitis
Limbic Encephalitis 		26 0 1 1.2E-03 0 0
CUI: C3711387
Disease: Autosomal Recessive Primary Microcephaly
Autosomal Recessive Primary Microcephaly 		26 0 1 1.2E-03 0 0
CUI: C0042063
Disease: Urogenital Abnormalities
Urogenital Abnormalities 		25 0 1 1.2E-03 0 0
CUI: C0431375
Disease: Classical Lissencephaly
Classical Lissencephaly 		24 0 1 1.2E-03 0 0
CUI: C0022541
Disease: Kearns-Sayre syndrome
Kearns-Sayre syndrome 		23 0 1 1.2E-03 0 0
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		23 0 1 1.2E-03 0 0
CUI: C0549393
Disease: Alcohol problem
Alcohol problem 		23 0 1 1.2E-03 0 0
CUI: C0949445
Disease: Cervical Dystonia
Cervical Dystonia 		23 0 1 1.2E-03 0 0
CUI: C1955690
Disease: Extranodal marginal zone B-cell lymphoma
Extranodal marginal zone B-cell lymphoma 		23 0 1 1.2E-03 0 0