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: C0036904
Disease: Sexual desire disorder
Sexual desire disorder 		0 1 0 0 1 3.3E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 3.3E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.3E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 3.3E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 3.3E-03
CUI: C3641106
Disease: Congenital Bleeding Disorder
Congenital Bleeding Disorder 		0 2 0 0 1 3.3E-03
CUI: C4551693
Disease: Wolfram Syndrome 1
Wolfram Syndrome 1 		0 4 0 0 1 3.3E-03
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		34 0 1 8.0E-04 0 0
CUI: C0085636
Disease: Photophobia
Photophobia 		31 0 1 8.0E-04 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome 		31 0 1 8.0E-04 0 0
CUI: C1631597
Disease: VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) 		30 0 1 8.1E-04 0 0
CUI: C1141890
Disease: Congenital long QT syndrome
Congenital long QT syndrome 		29 0 1 8.1E-04 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		28 0 1 8.1E-04 0 0
CUI: C3887506
Disease: Hyperkinesia
Hyperkinesia 		28 0 1 8.1E-04 0 0
CUI: C0205711
Disease: Pelizaeus-Merzbacher Disease
Pelizaeus-Merzbacher Disease 		27 0 1 8.1E-04 0 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		26 0 1 8.1E-04 0 0
CUI: C0849748
Disease: caruncle
caruncle 		25 0 1 8.1E-04 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		25 0 1 8.1E-04 0 0
CUI: C0431375
Disease: Classical Lissencephaly
Classical Lissencephaly 		24 0 1 8.1E-04 0 0
CUI: C3899503
Disease: Congenital hypogonadotropic hypogonadism
Congenital hypogonadotropic hypogonadism 		23 0 1 8.1E-04 0 0
CUI: C0023092
Disease: Lassa Fever
Lassa Fever 		22 0 1 8.1E-04 0 0
CUI: C0751602
Disease: Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Dominant Spastic Paraplegia 		22 0 1 8.1E-04 0 0
CUI: C0015624
Disease: Fanconi Syndrome
Fanconi Syndrome 		21 0 1 8.1E-04 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		21 0 1 8.1E-04 0 0
CUI: C1837454
Disease: SPINOCEREBELLAR ATAXIA 8
SPINOCEREBELLAR ATAXIA 8 		21 0 1 8.1E-04 0 0