DMGDH, dimethylglycine dehydrogenase, 29958

N. diseases: 15; N. variants: 25
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1853892
Disease: Dimethylglycine Dehydrogenase Deficiency
Dimethylglycine Dehydrogenase Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1 2 0.700 limited 1.000 5 1 1997 2016
CUI: C0005890
Disease: Body Height
Body Height 		phenotype Organism Attribute 1903 3972 0.100 None 1.000 1 1 2019 2019
CUI: C4049919
Disease: Insulin Sensitivity Measurement
Insulin Sensitivity Measurement 		phenotype Laboratory Procedure 14 32 0.100 None 1.000 1 1 2013 2013
CUI: C0455308
Disease: Serum selenium measurement
Serum selenium measurement 		phenotype Laboratory Procedure 5 8 0.100 None 1.000 1 3 2013 2013
CUI: C0373721
Disease: Selenium measurement
Selenium measurement 		phenotype Laboratory Procedure 7 17 0.100 None 1.000 1 9 2015 2015
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		disease Neoplasms Neoplastic Process 3111 6892 0.100 None 1.000 1 2 2017 2017
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		phenotype Diagnostic Procedure 399 1033 0.100 None 1.000 1 1 2019 2019
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		phenotype Finding 228 43 0.100 None 0
CUI: C4732768
Disease: Elevated N,N-dimethylglycine level
Elevated N,N-dimethylglycine level 		phenotype Finding 1 0.100 None 0
CUI: C4477064
Disease: Fish odor
Fish odor 		phenotype Sign or Symptom 1 0.100 None 0
CUI: C4025573
Disease: Increased muscle fatiguability
Increased muscle fatiguability 		phenotype Finding 9 3 0.100 None 0
CUI: C4022922
Disease: Abnormal enzyme/coenzyme activity
Abnormal enzyme/coenzyme activity 		phenotype Finding 13 0.100 None 0
CUI: C4732769
Disease: Elevated urinary N,N-dimethylglycine level
Elevated urinary N,N-dimethylglycine level 		phenotype Finding 1 0.100 None 0
CUI: C0025521
Disease: Inborn Errors of Metabolism
Inborn Errors of Metabolism 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome; Congenital Abnormality 119 3 0.020 None 1.000 2 1999 2001
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		disease Digestive System Diseases Disease or Syndrome 1058 222 0.010 None 1.000 1 1 2017 2017