Disease #02892 (HHF7 (Hyperinsulinemic hypoglycemia, familial, 7), OMIM:610021)

Official abbreviation HHF7
Name Hyperinsulinemic hypoglycemia, familial, 7
OMIM ID 610021
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SLC16A1
Associated tissues -
Disease features -
Remarks -