OBO ID: DOID:0070214
Term Name: familial hyperinsulinemic hypoglycemia 7 Search Ontology:
Synonyms:
  • EIHI
  • exercise-induced hyperinsulinemic hypoglycemia
  • exercise-induced hyperinsulinism
  • HHF7
  • hyperinsulinism due to monocarboxylate transporter 1 deficiency
  • hyperinsulinism due to SLC16A1 deficiency
Definition: A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of postexercise hypoglycemia with marked hyperinsulinism that has_material_basis_in mutation in the SLC16A1 gene on chromosome 1p13.2. https://www.ncbi.nlm.nih.gov/pubmed/17701893
References:
Ontology: Human Disease   ( DOID:0070214 )
Relationships
is a type of:
OTHER familial hyperinsulinemic hypoglycemia 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC16A1 Hyperinsulinemic hypoglycemia, familial, 7 610021
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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