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Human Disease

familial hyperinsulinemic hypoglycemia 8

Term ID
DOID:0081328
Synonyms
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 )
Relationships
is a type of
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Zebrafish Models
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