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| Term | familial hyperinsulinemic hypoglycemia 4 | ID (Ontology) | DOID:0070215 (Human Disease) |
| 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. | ||
| Also Known As | "HHF4" ; "hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency" ; "hyperinsulinism due to glutamodehydrogenase deficiency" (for all, see Synonyms field below) | ||
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autosomal genetic disease |__autosomal recessive disease____ hypoglycemia | |__hyperinsulinemic hypoglycemia__| familial hyperinsulinemic hypoglycemia 4 |
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autosomal recessive disease hyperinsulinemic hypoglycemia |
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GARD:2819 MIM:609975 ORDO:71212 |
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