Disease #00091 (HHF3 (HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3), OMIM:602485)

Official abbreviation HHF3
Name HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3
OMIM ID 602485
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GCK
Associated tissues -
Disease features -
Remarks -

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