loading...| Preferred Name | hyperinsulinemic hypoglycemia | |
| Synonyms |
nesidioblastosis hyperinsulinemia hypoglycemia persistent hyperinsulinemia hypoglycemia of infancy islet cell hyperplasia hyperinsulinemic hypoglycemia (disease) |
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| Definitions |
An inherited autosomal recessive syndrome characterized by the disorganized formation of new islets in the pancreas and congenital hyperinsulinism. It is due to focal hyperplasia of pancreatic islet cells budding off from the ductal structures and forming new islets of langerhans. Mutations in the islet cells involve the potassium channel gene kcnj11 or the atp-binding cassette transporter gene abcc8, both on chromosome 11. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0005803 |
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| altLabel |
nesidioblastosis hyperinsulinemia hypoglycemia persistent hyperinsulinemia hypoglycemia of infancy islet cell hyperplasia hyperinsulinemic hypoglycemia (disease) |
|
| definition |
An inherited autosomal recessive syndrome characterized by the disorganized formation of new islets in the pancreas and congenital hyperinsulinism. It is due to focal hyperplasia of pancreatic islet cells budding off from the ductal structures and forming new islets of langerhans. Mutations in the islet cells involve the potassium channel gene kcnj11 or the atp-binding cassette transporter gene abcc8, both on chromosome 11. |
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| has characteristic | ||
| has_exact_synonym |
hyperinsulinemia hypoglycemia persistent hyperinsulinemia hypoglycemia of infancy islet cell hyperplasia hyperinsulinemic hypoglycemia (disease) |
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| has_related_synonym |
nesidioblastosis |
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| IAO_0000233 | ||
| IAO_0000589 |
hyperinsulinemic hypoglycemia (disease) |
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| label |
hyperinsulinemic hypoglycemia |
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| prefixIRI |
MONDO:0005803 |
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| prefLabel |
hyperinsulinemic hypoglycemia |
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| textual definition |
An inherited autosomal recessive syndrome characterized by the disorganized formation of new islets in the pancreas and congenital hyperinsulinism. It is due to focal hyperplasia of pancreatic islet cells budding off from the ductal structures and forming new islets of langerhans. Mutations in the islet cells involve the potassium channel gene kcnj11 or the atp-binding cassette transporter gene abcc8, both on chromosome 11. |
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| subClassOf |