 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.
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
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| MeSH Number(s) |
C06.689.150 C16.614.200 C18.452.394.968.250 C18.452.394.984.200
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| Concept/Terms |
Congenital Hyperinsulinism- Congenital Hyperinsulinism
- Congenital Hyperinsulinisms
- Hyperinsulinisms, Congenital
- PHHI Hypoglycemia
- Hypoglycemia, PHHI
- Hypoglycemias, PHHI
- PHHI Hypoglycemias
- Hypoglycemia, Hyperinsulinemic, of Infancy
- Hyperinsulinemia Hypoglycemia of Infancy
- Infancy Hyperinsulinemia Hypoglycemia
- Infancy Hyperinsulinemia Hypoglycemias
- Hyperinsulinism, Congenital
- Persistent Hyperinsulinemia Hypoglycemia of Infancy
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Below are MeSH descriptors whose meaning is more general than "Congenital Hyperinsulinism".
Below are MeSH descriptors whose meaning is more specific than "Congenital Hyperinsulinism".
This graph shows the total number of publications written about "Congenital Hyperinsulinism" by people in UAMS Profiles by year, and whether "Congenital Hyperinsulinism" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 1 | 0 | 1 |
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Below are the most recent publications written about "Congenital Hyperinsulinism" by people in Profiles over the past ten years.
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