loading...| Preferred Name | Congenital Hyperinsulinism | |
| Synonyms |
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| 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. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_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. |
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| code |
C131425 |
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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. |
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| in_subset |
http://purl.obolibrary.org/obo/NCIT_C90259 |
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| label |
Congenital Hyperinsulinism |
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| NCI_META_CUI |
CL521303 |
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| Preferred_Name |
Congenital Hyperinsulinism |
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| prefixIRI |
NCIT:C131425 |
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| prefLabel |
Congenital Hyperinsulinism |
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| Semantic_Type |
Disease or Syndrome |
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| subClassOf |