Disease #00063 (HHF1 (HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1), OMIM:256450)

Official abbreviation HHF1
Name HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1
OMIM ID 256450
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ABCC8
Associated tissues -
Disease features -
Remarks -

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