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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Metabolic Diseases (D008659)
..Starting node ..Glucose Metabolism Disorders (D044882)
Child Nodes:
........Diabetes Mellitus (D003920) 106
........Glyceraldehyde-3-phosphate dehydrogenase deficiency (C536837)
........Glycosuria (D006029) 2
........Hyperglycemia (D006943) 1
........Hyperinsulinism (D006946) 16
........Hypoglycemia (D007003) 15
Sister Nodes:
..Acid-Base Imbalance (D000137) 42
..ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2 (OMIM:606770)
..ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3 (OMIM:606771)
..Brain Diseases, Metabolic (D001928) 244
..Calcium Metabolism Disorders (D002128) 94
..DNA Repair-Deficiency Disorders (D049914) 95
..Glucose Metabolism Disorders (D044882) 137
..Hyperlactatemia (D065906)
..Hypermanganesemia with Dystonia Polycythemia and Cirrhosis (C548016)
..Iron Metabolism Disorders (D019189) 23
..Lipid Metabolism Disorders (D052439) 189
..Malabsorption Syndromes (D008286) 29
..Metabolic Syndrome X (D024821) 1
..Metabolism, Inborn Errors (D008661) 886
..Mitochondrial Diseases (D028361) 114
..Phosphorus Metabolism Disorders (D010760) 25
..Porphyrias (D011164) 18
..Proteostasis Deficiencies (D057165) 55
..SHORT syndrome (C537327)
..Skin Diseases, Metabolic (D012875) 33
..Wasting Syndrome (D019282) 1
..Water-Electrolyte Imbalance (D014883) 31
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, 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: Genes:
Phenotypes
Disease Causing ClinVar Variants