MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, UMDF: 1= Disease, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, Myopathy, SANDO
Disease Browser
Parent Node:
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Metabolic Diseases (D008659)
..Starting node
..expand
Glucose Metabolism Disorders (D044882)

       Child Nodes:
........expandDiabetes Mellitus (D003920) Child106  LSDB C:3
........expandGlyceraldehyde-3-phosphate dehydrogenase deficiency (C536837)
........expandGlycosuria (D006029) Child2
........expandHyperglycemia (D006943) Child1
........expandHyperinsulinism (D006946) Child16
........expandHypoglycemia (D007003) Child15  LSDB C:3



 Sister Nodes: 
..expandAcid-Base Imbalance (D000137) Child42  LSDB C:10
..expandADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2 (OMIM:606770)
..expandADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3 (OMIM:606771)
..expandBrain Diseases, Metabolic (D001928) Child244  LSDB C:29
..expandCalcium Metabolism Disorders (D002128) Child94
..expandDNA Repair-Deficiency Disorders (D049914) Child95  LSDB C:1
..expandGlucose Metabolism Disorders (D044882) Child137  LSDB C:6
..expandHyperlactatemia (D065906)
..expandHypermanganesemia with Dystonia Polycythemia and Cirrhosis (C548016)
..expandIron Metabolism Disorders (D019189) Child23  LSDB C:1
..expandLipid Metabolism Disorders (D052439) Child189  LSDB C:9
..expandMalabsorption Syndromes (D008286) Child29
..expandMetabolic Syndrome X (D024821) Child1
..expandMetabolism, Inborn Errors (D008661) Child886  LSDB C:47
..expandMitochondrial Diseases (D028361) Child114  LSDB C:68
..expandPhosphorus Metabolism Disorders (D010760) Child25
..expandPorphyrias (D011164) Child18
..expandProteostasis Deficiencies (D057165) Child55
..expandSHORT syndrome (C537327)
..expandSkin Diseases, Metabolic (D012875) Child33
..expandWasting Syndrome (D019282) Child1
..expandWater-Electrolyte Imbalance (D014883) Child31
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:4685
Name:Glucose Metabolism Disorders
Definition:Pathological conditions in which the BLOOD GLUCOSE cannot be maintained within the normal range, such as in HYPOGLYCEMIA and HYPERGLYCEMIA. Etiology of these disorders varies. Plasma glucose concentration is critical to survival for it is the predominant fuel for the CENTRAL NERVOUS SYSTEM.
Alternative IDs:
ParentIDs:MESH:D008659
TreeNumbers:C18.452.394
Synonyms:Disorder, Glucose Metabolic |Disorder, Glucose Metabolism |Disorders, Glucose Metabolic |Disorders, Glucose Metabolism |Glucose Metabolic Disorder |Glucose Metabolic Disorders |Glucose Metabolism Disorder |Metabolic Disorder, Glucose |Metabolic Disorders, Glucos
Slim Mappings:Metabolic disease
Reference: MedGen: D044882
MeSH: D044882
OMIM:
MSeqDR LSDB:
MSeqDR has 6 matches in descendants: 00102; 00105; 00146; 00156; 00440; 00466;  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal