Disease #01966 (hhf1 (hypoglycemia, hyperinsulinemic, familial, type 1(HHF-1)), OMIM:256450)

Official abbreviation hhf1
Name hypoglycemia, hyperinsulinemic, familial, type 1(HHF-1)
OMIM ID 256450
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ABCC8
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A