loading...| Preferred Name | Congenital Hyperinsulinism | |
| Synonyms |
Neonatal Hyperinsulinism Nesidioblastosis Congenital Hyperinsulinism Hyperinsulinemic Hypoglycemia Hyperinsulinemia of Infancy HHI |
|
| Definitions |
An etiologically heterogenous condition resulting in dysregulated insulin secretion whose cause is present from birth. It is the most common cause of persistent hypoglycemia in neonates, infants and children. |
|
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C131425 |
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| ALT_DEFINITION |
An etiologically heterogenous condition resulting in dysregulated insulin secretion whose cause is present from birth. It is the most common cause of persistent hypoglycemia in neonates, infants and children. |
|
| code |
C131425 |
|
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118467 |
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| Contributing_Source |
Cellosaurus NICHD |
|
| DEFINITION |
An etiologically heterogenous condition resulting in dysregulated insulin secretion whose cause is present from birth. It is the most common cause of persistent hypoglycemia in neonates, infants and children. |
|
| FULL_SYN |
Neonatal Hyperinsulinism Nesidioblastosis Congenital Hyperinsulinism Hyperinsulinemic Hypoglycemia Hyperinsulinemia of Infancy HHI |
|
| label |
Congenital Hyperinsulinism |
|
| NCI_META_CUI |
CL521303 |
|
| Preferred_Name |
Congenital Hyperinsulinism |
|
| prefixIRI |
Thesaurus:C131425 |
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| Semantic_Type |
Disease or Syndrome |
|
| subClassOf |