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 -
Date created 2023-06-16 09:17:38 +00:00 (UTC)
Date last edited N/A

  Powered by LOVD v.3.0 Build 30
LOVD software ©2004-2024 Leiden University Medical Center 		There are currently no updates.