Disease #02429 (HHF3 (hypoglycemia, hyperinsulinemic, familial, type 3 (HHF-3)), OMIM:602485)
Official abbreviation |
HHF3 |
Name |
hypoglycemia, hyperinsulinemic, familial, type 3 (HHF-3) |
OMIM ID |
602485 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
GCK |
Associated tissues |
- |
Disease features |
autosomal dominant |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|