Preferred Name | hyperinsulinemic hypoglycemia, familial, 1 | |
Synonyms |
hyperinsulinism, congenital persistent hyperinsulinemic hypoglycemia of infancy HHF1 hypoglycemia, hyperinsulinemic, of infancy Nesidioblastosis of pancreas hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia hyperinsulinism, familial, with pancreatic Nesidioblastosis hyperinsulinemic hypoglycemia, familial, 1 hyperinsulinemic hypoglycemia due to SUR1 deficiency hyperinsulinemic hypoglycemia, familial, type 1 hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8 ABCC8 hyperinsulinemic hypoglycemia (disease) |
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Definitions |
Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the ABCC8 gene. |
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ID |
http://purl.obolibrary.org/obo/MONDO_0009734 |
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altLabel |
hyperinsulinism, congenital persistent hyperinsulinemic hypoglycemia of infancy HHF1 hypoglycemia, hyperinsulinemic, of infancy Nesidioblastosis of pancreas hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia hyperinsulinism, familial, with pancreatic Nesidioblastosis hyperinsulinemic hypoglycemia, familial, 1 hyperinsulinemic hypoglycemia due to SUR1 deficiency hyperinsulinemic hypoglycemia, familial, type 1 hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8 ABCC8 hyperinsulinemic hypoglycemia (disease) |
|
definition |
Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the ABCC8 gene. |
|
has_exact_synonym |
hyperinsulinemic hypoglycemia, familial, 1 hyperinsulinemic hypoglycemia due to SUR1 deficiency hyperinsulinemic hypoglycemia, familial, type 1 hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8 ABCC8 hyperinsulinemic hypoglycemia (disease) |
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has_related_synonym |
hyperinsulinism, congenital persistent hyperinsulinemic hypoglycemia of infancy HHF1 hypoglycemia, hyperinsulinemic, of infancy Nesidioblastosis of pancreas hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia hyperinsulinism, familial, with pancreatic Nesidioblastosis |
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label |
hyperinsulinemic hypoglycemia, familial, 1 |
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prefixIRI |
MONDO:0009734 |
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prefLabel |
hyperinsulinemic hypoglycemia, familial, 1 |
|
textual definition |
Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the ABCC8 gene. |
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subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.obolibrary.org/obo/MONDO_0009734 | EFO | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0009734 | MONDO | SAME_URI | |
http://purl.bioontology.org/ontology/OMIM/256450 | OMIM | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0009734 | EFO | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0009734 | MONDO | LOOM |