Search Ontology:
Human Disease
familial hyperinsulinemic hypoglycemia 8
- Term ID
- DOID:0081328
- Synonyms
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- Definition
- A hyperinsulinemic hypoglycemia characterized by protein-related hypoglycemia and persistent mild hyperammonemia and that has_material_basis_in homozygous mutation in the SLC25A36 gene on chromosome 3q23. https://pubmed.ncbi.nlm.nih.gov/34971397/
- References
- Ontology
- Human Disease ( DOID:0081328 )
- is a type of
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Genes Involved
Zebrafish Models