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: C0342765
Disease: D-Glyceric aciduria
D-Glyceric aciduria 		1 0 1 0.50 0 0
CUI: C1291386
Disease: D-glycericacidemia
D-glycericacidemia 		1 0 1 0.50 0 0
CUI: C0020501
Disease: Primary Hyperoxaluria
Primary Hyperoxaluria 		16 11 1 5.9E-02 4 6.5E-02
CUI: C0751748
Disease: Nonketotic Hyperglycinemia
Nonketotic Hyperglycinemia 		21 0 1 4.5E-02 0 0
CUI: C0268164
Disease: Primary hyperoxaluria, type I
Primary hyperoxaluria, type I 		27 169 1 3.6E-02 1 4.5E-03
CUI: C0151818
Disease: Opisthotonus
Opisthotonus 		32 0 1 3.0E-02 0 0
CUI: C0238621
Disease: Aminoaciduria
Aminoaciduria 		68 0 2 2.9E-02 0 0
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE 		33 0 1 2.9E-02 0 0
CUI: C0020500
Disease: Hyperoxaluria
Hyperoxaluria 		49 0 1 2.0E-02 0 0
CUI: C2931788
Disease: Atypical Hemolytic Uremic Syndrome
Atypical Hemolytic Uremic Syndrome 		56 0 1 1.8E-02 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis 		85 0 1 1.2E-02 0 0
CUI: C0426970
Disease: Spastic Quadriplegia
Spastic Quadriplegia 		86 0 1 1.1E-02 0 0
CUI: C0019061
Disease: Hemolytic-Uremic Syndrome
Hemolytic-Uremic Syndrome 		110 0 1 9.0E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		112 0 1 8.8E-03 0 0
CUI: C0027709
Disease: Nephrocalcinosis
Nephrocalcinosis 		118 20 1 8.4E-03 2 2.7E-02
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		152 0 1 6.5E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		156 0 1 6.4E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 5.9E-03 0 0
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi 		190 0 1 5.2E-03 0 0
CUI: C0018965
Disease: Hematuria
Hematuria 		235 0 1 4.2E-03 0 0
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection 		237 0 1 4.2E-03 0 0
CUI: C0392525
Disease: Nephrolithiasis
Nephrolithiasis 		242 99 1 4.1E-03 2 1.3E-02
CUI: C0456070
Disease: Growth delay
Growth delay 		244 0 1 4.1E-03 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus 		265 0 1 3.8E-03 0 0
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		271 0 1 3.7E-03 0 0