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: C0751776
Disease: Atypical Inclusion-Body Disease
Atypical Inclusion-Body Disease 		17 0 17 0.18 0 0
CUI: C0751777
Disease: Familial Progressive Myoclonic Epilepsy
Familial Progressive Myoclonic Epilepsy 		17 0 17 0.18 0 0
CUI: C0751780
Disease: Biotin-Responsive Encephalopathy
Biotin-Responsive Encephalopathy 		17 0 17 0.18 0 0
CUI: C0751782
Disease: May-White Syndrome
May-White Syndrome 		17 0 17 0.18 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 19 0.18 0 0
CUI: C0751779
Disease: Action Myoclonus-Renal Failure Syndrome
Action Myoclonus-Renal Failure Syndrome 		20 0 17 0.17 0 0
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive 		48 0 21 0.17 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		156 0 31 0.14 0 0
CUI: C0024408
Disease: Machado-Joseph Disease
Machado-Joseph Disease 		135 0 27 0.13 0 0
CUI: C0752120
Disease: Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1 		102 0 23 0.13 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 13 0.13 0 0
CUI: C0752124
Disease: Spinocerebellar Ataxia Type 6 (disorder)
Spinocerebellar Ataxia Type 6 (disorder) 		64 0 18 0.13 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 26 0.13 0 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary 		35 0 14 0.12 0 0
CUI: C0751785
Disease: Unverricht-Lundborg Syndrome
Unverricht-Lundborg Syndrome 		56 0 16 0.12 0 0
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia Type 7 		78 0 18 0.12 0 0
CUI: C0019212
Disease: Hepatorenal Syndrome
Hepatorenal Syndrome 		25 0 12 0.11 0 0
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular 		86 0 17 0.10 0 0
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases 		66 0 15 0.10 0 0
CUI: C0271390
Disease: Nystagmus, End-Position
Nystagmus, End-Position 		26 0 11 1.0E-01 0 0
CUI: C1619727
Disease: Decompensated cirrhosis of liver
Decompensated cirrhosis of liver 		52 0 13 9.7E-02 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2 		76 0 15 9.6E-02 0 0
CUI: C0221271
Disease: Elastosis perforans serpiginosa
Elastosis perforans serpiginosa 		66 0 14 9.5E-02 0 0
CUI: C4551504
Disease: Oculocutaneous albinism type 1A
Oculocutaneous albinism type 1A 		21 0 10 9.4E-02 0 0
CUI: C1839259
Disease: Bulbo-Spinal Atrophy, X-Linked
Bulbo-Spinal Atrophy, X-Linked 		126 0 19 9.4E-02 0 0