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: C0149877
Disease: Hypoglycemic encephalopathy
Hypoglycemic encephalopathy 		1 0 1 0.12 0 0
CUI: C0267430
Disease: Noninfectious colitis
Noninfectious colitis 		1 0 1 0.12 0 0
CUI: C0342970
Disease: Increased oxygen demand
Increased oxygen demand 		1 0 1 0.12 0 0
CUI: C0345903
Disease: Anal skin tag
Anal skin tag 		1 0 1 0.12 0 0
CUI: C1321275
Disease: Non-specific colitis
Non-specific colitis 		1 0 1 0.12 0 0
CUI: C1332259
Disease: Adenocarcinoma of anal canal
Adenocarcinoma of anal canal 		1 0 1 0.12 0 0
CUI: C1333110
Disease: Colorectal High Grade Intraepithelial Neoplasia
Colorectal High Grade Intraepithelial Neoplasia 		1 0 1 0.12 0 0
CUI: C1456270
Disease: Fatty acid oxidation disorder
Fatty acid oxidation disorder 		1 0 1 0.12 0 0
CUI: C1860081
Disease: Medium chain dicarboxylic aciduria
Medium chain dicarboxylic aciduria 		1 0 1 0.12 0 0
CUI: C1864948
Disease: Hyperinsulinemic Hypoglycemia, Familial, 4
Hyperinsulinemic Hypoglycemia, Familial, 4 		1 0 1 0.12 0 0
CUI: C1970173
Disease: Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of
Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of 		1 0 1 0.12 0 0
CUI: C3532934
Disease: Mild expressive language delay
Mild expressive language delay 		1 0 1 0.12 0 0
CUI: C4022414
Disease: Elevated urinary 3-hydroxybutyric acid
Elevated urinary 3-hydroxybutyric acid 		1 0 1 0.12 0 0
CUI: C4280763
Disease: Increased C-peptide level
Increased C-peptide level 		1 0 1 0.12 0 0
CUI: C0149854
Disease: Cerebellar hemorrhage
Cerebellar hemorrhage 		2 0 1 0.11 0 0
CUI: C0220711
Disease: Long chain acyl-CoA dehydrogenase deficiency
Long chain acyl-CoA dehydrogenase deficiency 		2 0 1 0.11 0 0
CUI: C0268576
Disease: Hyperleucinemia
Hyperleucinemia 		2 0 1 0.11 0 0
CUI: C0751486
Disease: Reye-Like Syndrome
Reye-Like Syndrome 		2 0 1 0.11 0 0
CUI: C0849888
Disease: psychological disturbance
psychological disturbance 		2 0 1 0.11 0 0
CUI: C1332262
Disease: Anal canal squamous cell carcinoma
Anal canal squamous cell carcinoma 		2 0 1 0.11 0 0
CUI: C1829742
Disease: Fatty acid oxidation defects
Fatty acid oxidation defects 		2 0 1 0.11 0 0
CUI: C3554691
Disease: HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES
HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES 		2 0 1 0.11 0 0
CUI: C4023117
Disease: Decreased plasma total carnitine
Decreased plasma total carnitine 		2 0 1 0.11 0 0
CUI: C4280773
Disease: Increased circulating free fatty acid level
Increased circulating free fatty acid level 		2 0 2 0.25 0 0
CUI: C4747517
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20 		2 0 1 0.11 0 0