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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: Glucose Metabolism Disorders (D044882)
..Starting node ..Hyperinsulinism (D006946)
Child Nodes:
........Congenital Hyperinsulinism (D044903) 2
........Homozygous 11p15-p14 Deletion Syndrome (C564701)
........Hyperinsulinemic hypoglycemia, familial, 3 (C538374)
........Hyperinsulinemic Hypoglycemia, Familial, 4 (C566493)
........Hyperinsulinemic Hypoglycemia, Familial, 5 (C566494)
........Hyperinsulinemic hypoglycemia, familial, 6 (C538375)
........Hyperinsulinemic hypoglycemia, familial, 7 (C538376)
........Insulin Resistance (D007333) 6
Sister Nodes:
..Diabetes Mellitus (D003920) 106
..Glyceraldehyde-3-phosphate dehydrogenase deficiency (C536837)
..Glycosuria (D006029) 2
..Hyperglycemia (D006943) 1
..Hyperinsulinism (D006946) 16
..Hypoglycemia (D007003) 15
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5395
Name:	Hyperinsulinism
Definition:	A syndrome with excessively high INSULIN levels in the BLOOD. It may cause HYPOGLYCEMIA. Etiology of hyperinsulinism varies, including hypersecretion of a beta cell tumor (INSULINOMA); autoantibodies against insulin (INSULIN ANTIBODIES); defective insulin receptor (INSULIN RESISTANCE); or overuse of exogenous insulin or HYPOGLYCEMIC AGENTS.
Alternative IDs:
ParentIDs:	MESH:D044882
TreeNumbers:	C18.452.394.968
Synonyms:	Compensatory Hyperinsulinemia \|Endogenous Hyperinsulinism \|Exogenous Hyperinsulinism \|Hyperinsulinemia \|Hyperinsulinemia, Compensatory \|Hyperinsulinism, Endogenous \|Hyperinsulinism, Exogenous
Slim Mappings:	Metabolic disease
Reference:	MedGen: D006946 MeSH: D006946 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants