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: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		209 0 1 4.8E-03 0 0
CUI: C0002534
Disease: Renal Aminoacidurias
Renal Aminoacidurias 		1 0 1 1.00 0 0
CUI: C0004134
Disease: Ataxia
Ataxia 		868 0 1 1.2E-03 0 0
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		560 0 1 1.8E-03 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		842 0 1 1.2E-03 0 0
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		3177 0 1 3.1E-04 0 0
CUI: C0017638
Disease: Glioma
Glioma 		3097 0 1 3.2E-04 0 0
CUI: C0020458
Disease: Hyperhidrosis disorder
Hyperhidrosis disorder 		114 0 1 8.8E-03 0 0
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia 		420 0 1 2.4E-03 0 0
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		144 0 1 6.9E-03 0 0
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		3806 0 1 2.6E-04 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		967 0 1 1.0E-03 0 0
CUI: C0036572
Disease: Seizures
Seizures 		2152 0 1 4.6E-04 0 0
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		429 0 1 2.3E-03 0 0
CUI: C0037268
Disease: Skin Abnormalities
Skin Abnormalities 		106 0 1 9.4E-03 0 0
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		820 0 1 1.2E-03 0 0
CUI: C0085584
Disease: Encephalopathies
Encephalopathies 		457 0 1 2.2E-03 0 0
CUI: C0085682
Disease: Hypophosphatemia
Hypophosphatemia 		69 0 1 1.4E-02 0 0
CUI: C0162666
Disease: Mitochondrial Encephalomyopathies
Mitochondrial Encephalomyopathies 		53 0 1 1.9E-02 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 1 7.0E-03 0 0
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		473 0 1 2.1E-03 0 0
CUI: C0235874
Disease: Disease Exacerbation
Disease Exacerbation 		166 0 1 6.0E-03 0 0
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy 		454 0 1 2.2E-03 0 0
CUI: C0242292
Disease: McCune-Albright Syndrome
McCune-Albright Syndrome 		45 0 1 2.2E-02 0 0
CUI: C0268583
Disease: Methylmalonic acidemia
Methylmalonic acidemia 		44 0 1 2.3E-02 0 0