Search Ontology:
Human Disease

familial hyperinsulinemic hypoglycemia 4

Term ID
DOID:0070215
Synonyms
  • HHF4
  • hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
  • hyperinsulinism due to glutamodehydrogenase deficiency
  • hyperinsulinism due to SCHAD deficiency
  • hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
Definition
A hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of hyperinsulinemic hypoglycemia with seizures that has_material_basis_in mutation in the HADH gene on chromosome 4q25. https://www.ncbi.nlm.nih.gov/pubmed/11489939
References
Ontology
Human Disease   ( DOID:0070215 )
Relationships
is a type of
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Genes Involved
Zebrafish Models