Persistent Hyperinsulinemia Hypoglycemia of Infancy
"Persistent Hyperinsulinemia Hypoglycemia of Infancy" 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
|
| 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
- 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
|
Below are MeSH descriptors whose meaning is more general than "Persistent Hyperinsulinemia Hypoglycemia of Infancy".
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