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: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		96 0 1 1.6E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.7E-03 0 0
CUI: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
[D]Sleep disturbances (& [hypersomnia] or [insomnia]) 		69 0 1 1.7E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		68 0 1 1.7E-03 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		63 0 1 1.7E-03 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		62 0 1 1.7E-03 0 0
CUI: C3496069
Disease: cocaine use
cocaine use 		59 0 1 1.7E-03 0 0
CUI: C0683322
Disease: Mental impairment
Mental impairment 		58 0 1 1.7E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		57 0 1 1.7E-03 0 0
CUI: C0017495
Disease: Gerstmann-Straussler-Scheinker Disease
Gerstmann-Straussler-Scheinker Disease 		56 0 1 1.7E-03 0 0
CUI: C0023015
Disease: Language Disorders
Language Disorders 		56 0 1 1.7E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		52 0 1 1.7E-03 0 0
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		52 0 1 1.7E-03 0 0
CUI: C0233523
Disease: Antisocial behavior
Antisocial behavior 		51 0 1 1.8E-03 0 0
CUI: C0220748
Disease: Cartilage-hair hypoplasia
Cartilage-hair hypoplasia 		49 0 1 1.8E-03 0 0
CUI: C0393639
Disease: Hashimoto's encephalitis
Hashimoto's encephalitis 		47 0 1 1.8E-03 0 0
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses 		45 0 1 1.8E-03 0 0
CUI: C0220766
Disease: Congenital hypoplasia of adrenal gland
Congenital hypoplasia of adrenal gland 		45 0 1 1.8E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		45 0 1 1.8E-03 0 0
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures 		45 0 1 1.8E-03 0 0
CUI: C1852502
Disease: CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT 		45 0 1 1.8E-03 0 0
CUI: C0029438
Disease: Massive Osteolyses
Massive Osteolyses 		44 0 1 1.8E-03 0 0
CUI: C0017919
Disease: Glycogen Storage Disease
Glycogen Storage Disease 		43 0 1 1.8E-03 0 0
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		43 0 1 1.8E-03 0 0
CUI: C0007965
Disease: Chediak-Higashi Syndrome
Chediak-Higashi Syndrome 		41 0 1 1.8E-03 0 0