Source: ALL
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: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder) 		20 0 1 2.7E-04 0 0
CUI: C3468114
Disease: Juvenile amyotrophic lateral sclerosis
Juvenile amyotrophic lateral sclerosis 		20 0 1 2.7E-04 0 0
CUI: C0241688
Disease: Peripheral visual field loss
Peripheral visual field loss 		19 0 1 2.7E-04 0 0
CUI: C0751884
Disease: Congenital Myasthenic Syndromes, Presynaptic
Congenital Myasthenic Syndromes, Presynaptic 		19 0 1 2.7E-04 0 0
CUI: C1969156
Disease: EEG with burst suppression
EEG with burst suppression 		19 0 1 2.7E-04 0 0
CUI: C4317295
Disease: Congenital disorder of glycosylation type 1s
Congenital disorder of glycosylation type 1s 		19 0 1 2.7E-04 0 0
CUI: C4551631
Disease: Cystic liver disease
Cystic liver disease 		19 0 1 2.7E-04 0 0
CUI: C0282525
Disease: Adrenoleukodystrophy, Neonatal
Adrenoleukodystrophy, Neonatal 		18 0 1 2.7E-04 0 0
CUI: C0431565
Disease: Hamartoma of tongue
Hamartoma of tongue 		18 0 1 2.7E-04 0 0
CUI: C1740801
Disease: Exaggerated startle response
Exaggerated startle response 		18 0 1 2.7E-04 0 0
CUI: C1834433
Disease: Obsessive-compulsive trait
Obsessive-compulsive trait 		18 0 1 2.7E-04 0 0
CUI: C1837496
Disease: Axonal degeneration
Axonal degeneration 		17 0 1 2.7E-04 0 0
CUI: C1844906
Disease: Broad finger
Broad finger 		17 0 1 2.7E-04 0 0
CUI: C0036069
Disease: Saldino-Noonan Syndrome
Saldino-Noonan Syndrome 		16 0 1 2.7E-04 0 0
CUI: C0158551
Disease: Embryonal nuclear cataract (disorder)
Embryonal nuclear cataract (disorder) 		16 0 1 2.7E-04 0 0
CUI: C0393556
Disease: Complicated hereditary spastic paraplegia
Complicated hereditary spastic paraplegia 		16 0 1 2.7E-04 0 0
CUI: C1839071
Disease: Spermatogenic Failure, Nonobstructive, Y-Linked
Spermatogenic Failure, Nonobstructive, Y-Linked 		16 0 1 2.7E-04 0 0
CUI: C3501611
Disease: Mental Retardation, X-Linked Nonsyndromic
Mental Retardation, X-Linked Nonsyndromic 		16 0 1 2.7E-04 0 0
CUI: C1839025
Disease: Decreased light- and dark-adapted electroretinogram amplitude
Decreased light- and dark-adapted electroretinogram amplitude 		15 0 1 2.7E-04 0 0
CUI: C1847352
Disease: POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
POLYMICROGYRIA, BILATERAL FRONTOPARIETAL 		15 0 1 2.7E-04 0 0
CUI: C2749688
Disease: Abnormal isoelectric focusing of serum transferrin
Abnormal isoelectric focusing of serum transferrin 		15 0 1 2.7E-04 0 0
CUI: C2936406
Disease: alpha-Dystroglycanopathies
alpha-Dystroglycanopathies 		15 0 1 2.7E-04 0 0
CUI: C3279397
Disease: Very long chain fatty acid accumulation
Very long chain fatty acid accumulation 		15 0 1 2.7E-04 0 0
CUI: C3840214
Disease: High-functioning autism
High-functioning autism 		15 0 1 2.7E-04 0 0
CUI: C4022849
Disease: Absent thumbnail
Absent thumbnail 		15 0 1 2.7E-04 0 0