Disease #02394 (HHF2 (hypoglycemia, hyperinsulinemic, familial, type 2 (HHF-2)), OMIM:601820)
Official abbreviation |
HHF2 |
Name |
hypoglycemia, hyperinsulinemic, familial, type 2 (HHF-2) |
OMIM ID |
601820 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
KCNJ11 |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
Individuals
|
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