Congenital Hyperinsulinism

"Congenital Hyperinsulinism" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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).

Descriptor ID	D044903
MeSH Number(s)	C06.689.150 C16.614.200 C18.452.394.968.250 C18.452.394.984.200
Concept/Terms	Congenital Hyperinsulinism Congenital Hyperinsulinism Congenital Hyperinsulinisms Hyperinsulinisms, Congenital Hyperinsulinemia Hypoglycemia of Infancy Infancy Hyperinsulinemia Hypoglycemias Hyperinsulinemic Hypoglycemia, Persistent Hyperinsulinemic Hypoglycemias, Persistent Hypoglycemia, Persistent Hyperinsulinemic Hypoglycemias, Persistent Hyperinsulinemic Persistent Hyperinsulinemic Hypoglycemias Hyperinsulinism, Congenital Hyperinsulinism, Familial Familial Hyperinsulinisms Hyperinsulinisms, Familial PHHI Hypoglycemia Hypoglycemia, PHHI Hypoglycemias, PHHI PHHI Hypoglycemias Hypoglycemia, Hyperinsulinemic, of Infancy Infancy Hyperinsulinemia Hypoglycemia Neonatal Hyperinsulinism Persistent Hyperinsulinemia Hypoglycemia of Infancy Persistent Hyperinsulinemic Hypoglycemia Familial Hyperinsulinism Hyperinsulinism, Neonatal Hyperinsulinisms, Neonatal Neonatal Hyperinsulinisms Hyperinsulinemic Hypoglycemia, Familial, 2 Hyperinsulinemic Hypoglycemia, Familial, 2 Familial Hyperinsulinemic Hypoglycemia 1 Familial Hyperinsulinemic Hypoglycemia 1 Hyperinsulinemic Hypoglycemia, Familial, 1 Hyperinsulinemic Hypoglycemia Due to Focal Adenomatous Hyperplasia

Below are MeSH descriptors whose meaning is more general than "Congenital Hyperinsulinism".

Diseases [C]
Digestive System Diseases [C06]
Pancreatic Diseases [C06.689]
Congenital Hyperinsulinism [C06.689.150]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Infant, Newborn, Diseases [C16.614]
Congenital Hyperinsulinism [C16.614.200]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Glucose Metabolism Disorders [C18.452.394]
Hyperinsulinism [C18.452.394.968]
Congenital Hyperinsulinism [C18.452.394.968.250]
Hypoglycemia [C18.452.394.984]
Congenital Hyperinsulinism [C18.452.394.984.200]

Below are MeSH descriptors whose meaning is related to "Congenital Hyperinsulinism".

Below are MeSH descriptors whose meaning is more specific than "Congenital Hyperinsulinism".

Congenital Hyperinsulinism
Nesidioblastosis

publications

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