raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:276525

Familial hyperinsulinism

Synonyms: FHI · Familial hyperinsulinemic hypoglycemia

Type
Category
Group
Group of disorders
Status
active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enFamilial hyperinsulinismFHI · Familial hyperinsulinemic hypoglycemia
frHyperinsulinisme familialFHI · Hypoglycémie hyperinsulinémique familiale
deHyperinsulinismus, familiärerFHI · Hypoglykämie, hyperinsulinämische, familiäre
esHiperinsulinismo familiarHipoglucemia hiperinsulinémica familiar
itIperinsulinismo familiareFHI · Ipoglicemia iperinsulinemica familiare
nlFamiliaal hyperinsulinismeFHI · Familiale hyperinsulinemische hypoglycemie
ptHiperinsulinismo familiar
plHiperinsulinizm rodzinnyFHI · Rodzinna hipoglikemia hiperinsulinemiczna
csFamiliární hyperinzulinismusFHI · Familiární hyperinzulinemická hypoglykémie
ukСімейний гіперінсулінізмСімейна гіперінсулінемічна гіпоглікемія · FHI
zh家族性高胰岛素血症家族性高胰岛素低血糖
trAilesel hiperinsülinizmFHI · Ailesel hiperinsülinemik hipoglisemi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0017182Evalidated
MONDO17182Evalidated
UMLSC5848294Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (2):

Children (4):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card