FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term leucine-sensitive hypoglycemia of infancy ID (Ontology) DOID:0112262 (Human Disease)
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.
Also Known As "leucine-induced hypoglycemia" ; "LIH"
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 Genes
 leucine-sensitive hypoglycemia of infancy      11
 for disease ribbon | leucine-sensitive hypoglycemia of infancy      11
 model of | leucine-sensitive hypoglycemia of infancy      11
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_____
glucose metabolism disease         |
 |__hypoglycemia___________________|
inherited metabolic disorder       |
 |__amino acid metabolic disorder__|
                                   leucine-sensitive hypoglycemia of infancy  11 rec.
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Is a autosomal dominant disease
amino acid metabolic disorder
hypoglycemia
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Synonyms
  • "leucine-induced hypoglycemia" EXACT
    "LIH" EXACT OMO:0003012
Secondary IDs
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GARD:9915
MIM:240800