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DO Term : familial hyperinsulinemic hypoglycemia 7 [DOID:0070214] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • MESH:C538376,
  • NCI:C131839,
  • EIHI,
  • exercise-induced hyperinsulinemic hypoglycemia,
  • OMIM:610021,
  • UMLS_CUI:C1864902,
  • hyperinsulinism due to monocarboxylate transporter 1 deficiency,
  • hyperinsulinism due to SLC16A1 deficiency,
  • 610021,
  • ORDO:165991,
  • exercise-induced hyperinsulinism,
  • GARD:9932,
  • SNOMEDCT_US_2023_03_01:715830008,
  • HHF7
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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents