OBO ID: DOID:0112262 |
Term Name: | leucine-sensitive hypoglycemia of infancy | Search Ontology: | |
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Definition: | An amino acid metabolic disorder characterized by development of hypoglycemia after high-protein feedings or leucine infusion that has_material_basis_in heterozygous mutation in the SUR1 gene on chromosome 11p15.1. https://pubmed.ncbi.nlm.nih.gov/15356046/ | ||
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Ontology: | Human Disease ( DOID:0112262 ) |
OTHER leucine-sensitive hypoglycemia of infancy PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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