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: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		192 65 21 0.10 3 4.2E-02
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 15 1.0E-01 0 0
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia 		118 0 14 1.0E-01 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 6 9.8E-02 0 0
CUI: C0270846
Disease: Epileptic drop attack
Epileptic drop attack 		143 0 16 9.8E-02 0 0
CUI: C0037769
Disease: West Syndrome
West Syndrome 		149 0 16 9.5E-02 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		152 0 16 9.3E-02 0 0
CUI: C2748910
Disease: Rett Syndrome, Atypical
Rett Syndrome, Atypical 		11 0 4 9.3E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination 		59 0 8 9.2E-02 0 0
CUI: C0014550
Disease: Myoclonic Epilepsy
Myoclonic Epilepsy 		71 0 9 9.2E-02 0 0
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine 		24 0 5 9.1E-02 0 0
CUI: C1720416
Disease: Episodic ataxia type 2 (disorder)
Episodic ataxia type 2 (disorder) 		13 60 4 8.9E-02 5 7.8E-02
CUI: C0751122
Disease: Infantile Severe Myoclonic Epilepsy
Infantile Severe Myoclonic Epilepsy 		63 0 8 8.8E-02 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 16 8.8E-02 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 126 18 8.8E-02 3 2.3E-02
CUI: C0271390
Disease: Nystagmus, End-Position
Nystagmus, End-Position 		26 0 5 8.8E-02 0 0
CUI: C0034013
Disease: Precocious Puberty
Precocious Puberty 		139 0 14 8.7E-02 0 0
CUI: C1868682
Disease: Paroxysmal kinesigenic choreoathetosis
Paroxysmal kinesigenic choreoathetosis 		14 0 4 8.7E-02 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		205 0 19 8.6E-02 0 0
CUI: C0393588
Disease: Dystonia, Paroxysmal
Dystonia, Paroxysmal 		28 4 5 8.5E-02 1 8.3E-02
CUI: C0018991
Disease: Hemiplegia
Hemiplegia 		41 0 6 8.5E-02 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		149 0 14 8.2E-02 0 0
CUI: C1839333
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 		57 0 7 8.1E-02 0 0
CUI: C0220766
Disease: Congenital hypoplasia of adrenal gland
Congenital hypoplasia of adrenal gland 		45 0 6 8.0E-02 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 4 8.0E-02 0 0