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: C4022830
Disease: Heavy proteinuria
Heavy proteinuria 		2 0 2 0.50 0 0
CUI: C1850069
Disease: Undetectable visual evoked potentials
Undetectable visual evoked potentials 		6 0 2 0.25 0 0
CUI: C3553358
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 3
COENZYME Q10 DEFICIENCY, PRIMARY, 3 		1 0 1 0.25 0 0
CUI: C3714927
Disease: MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO 		1 0 1 0.25 0 0
CUI: C4022677
Disease: Female anorgasmia
Female anorgasmia 		1 0 1 0.25 0 0
CUI: C4310794
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53 		1 0 1 0.25 0 0
CUI: C0749201
Disease: Orthostatic syncope
Orthostatic syncope 		2 0 1 0.20 0 0
CUI: C1838877
Disease: Myoglobinuria, Recurrent
Myoglobinuria, Recurrent 		2 0 1 0.20 0 0
CUI: C1839436
Disease: Severe lactic acidosis
Severe lactic acidosis 		8 0 2 0.20 0 0
CUI: C1868524
Disease: Autonomic erectile dysfunction
Autonomic erectile dysfunction 		2 0 1 0.20 0 0
CUI: C2219848
Disease: Daytime somnolence
Daytime somnolence 		2 0 1 0.20 0 0
CUI: C4551502
Disease: HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		2 0 1 0.20 0 0
CUI: C4746986
Disease: ALPORT SYNDROME 1, X-LINKED
ALPORT SYNDROME 1, X-LINKED 		2 0 1 0.20 0 0
CUI: C0585544
Disease: Downbeat nystagmus
Downbeat nystagmus 		3 0 1 0.17 0 0
CUI: C0796221
Disease: MENTAL RETARDATION, X-LINKED 15
MENTAL RETARDATION, X-LINKED 15 		3 0 1 0.17 0 0
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		3 0 1 0.17 0 0
CUI: C1850534
Disease: Edema, generalized
Edema, generalized 		12 0 2 0.14 0 0
CUI: C4554651
Disease: Generalized Edema, CTCAE
Generalized Edema, CTCAE 		12 0 2 0.14 0 0
CUI: C0752324
Disease: Focal Tonic Seizures
Focal Tonic Seizures 		5 0 1 0.12 0 0
CUI: C4025212
Disease: Autonomic bladder dysfunction
Autonomic bladder dysfunction 		5 0 1 0.12 0 0
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		6 0 1 0.11 0 0
CUI: C1836149
Disease: Axial dystonia
Axial dystonia 		6 0 1 0.11 0 0
CUI: C3825926
Disease: Nephrotic syndrome in children
Nephrotic syndrome in children 		6 0 1 0.11 0 0
CUI: C0270733
Disease: Striatonigral Degeneration
Striatonigral Degeneration 		7 0 1 1.0E-01 0 0
CUI: C0264162
Disease: Camptocormia
Camptocormia 		8 0 1 9.1E-02 0 0