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	-
Date created	2023-06-16 08:24:55 +00:00 (UTC)
Date last edited	N/A

MVZ für Humangenetik Regensburg