ABCC8 mutants (HHF1)

Stable Identifier
R-HSA-5683203
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Participant Of
Disease
Name Identifier Synonyms
hyperinsulinemic hypoglycemia 13317 Islet cell hyperplasia, nesidioblastosis, persistent hyperinsulinemia hypoglycemia of infancy