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Congenital Hyperinsulinism MeSH Descriptor Data 2022


MeSH Heading
Congenital Hyperinsulinism
Tree Number(s)
C06.689.150
C16.614.200
C18.452.394.968.250
C18.452.394.984.200
Unique ID
D044903
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D044903
Scope Note
A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMIA; HYPERINSULINEMIA; SEIZURES; COMA; and often large BIRTH WEIGHT. Several sub-types exist with the most common, type 1, associated with mutations on an ATP-BINDING CASSETTE TRANSPORTERS (subfamily C, member 8).
Entry Term(s)
Familial Hyperinsulinemic Hypoglycemia 1
Familial Hyperinsulinism
Hyperinsulinemia Hypoglycemia of Infancy
Hyperinsulinemic Hypoglycemia Due to Focal Adenomatous Hyperplasia
Hyperinsulinemic Hypoglycemia, Familial, 1
Hyperinsulinemic Hypoglycemia, Familial, 2
Hyperinsulinemic Hypoglycemia, Persistent
Hyperinsulinism, Congenital
Hyperinsulinism, Familial
Hyperinsulinism, Neonatal
Hypoglycemia, Hyperinsulinemic, of Infancy
Infancy Hyperinsulinemia Hypoglycemia
Neonatal Hyperinsulinism
PHHI Hypoglycemia
Persistent Hyperinsulinemia Hypoglycemia of Infancy
Persistent Hyperinsulinemic Hypoglycemia
Previous Indexing
Chromosomes, Human, Pair 11 (1995-2003)
Hyperinsulinism (1977-2003)
Hypoglycemia (1977-2003)
See Also
ATP-Binding Cassette Transporters
Potassium Channels, Inwardly Rectifying
Public MeSH Note
2014; see PERSISTENT HYPERINSULINEMIA HYPOGLYCEMIA OF INFANCY 2004-2013
History Note
2014(2004)
Date Established
2004/01/01
Date of Entry
2003/07/09
Revision Date
2013/07/08
Congenital Hyperinsulinism Preferred
Hyperinsulinemic Hypoglycemia, Familial, 2 Narrower
Familial Hyperinsulinemic Hypoglycemia 1 Narrower
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