An instance of hyperinsulinism (disease) that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]
Synonyms: nesidioblastosis neonatal hyperinsulinism FHI hyperinsulinemia of infancy HHI hereditary hyperinsulinism (disease) congenital hyperinsulinism familial hyperinsulinemic hypoglycemia
Term information
- NCIT:C131425 (MONDO:equivalentTo)
- GARD:21053 (Orphanet:276525)
- Orphanet:276525 (MONDO:equivalentTo)
gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders