ORPHA:165985
Diazoxide-sensitive diffuse hyperinsulinism
Synonyms: Hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form
- Type
- Clinical group
- 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| Lang | Name | Synonyms |
|---|---|---|
| en | Diazoxide-sensitive diffuse hyperinsulinism | Hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form |
| fr | Hyperinsulinisme diffus sensible au diazoxide | Hypoglycémie hyperinsulinémique, forme diffuse sensible au diazoxide |
| de | Hyperinsulinismus, diffuser, Diazoxid-sensitiver | Hyperinsulinämische Hypoglykämie, Diazoxid-sensitive diffuse Form |
| es | Hiperinsulinismo difuso sensible al diazóxido | Hipoglucemia hiperinsulinémica, forma difusa sensible al diazóxido |
| it | Iperinsulinismo diffuso sensibile al diazossido | Ipoglicemia iperinsulinemica, forma diffusa sensibile al diazossido |
| nl | Diazoxidesensitief diffuus hyperinsulinisme | Hyperinsulinemische hypoglycemie, diazoxidesensitieve diffuse vorm |
| pt | Hiperinsulinismo difuso sensível ao diazóxido | |
| pl | Rozlany hiperinsulinizm wrażliwy na diazoksyd | Hipoglikemia hiperinsulinemiczna, forma rozlana wrażliwa na diazoksyd |
| cs | Difuzní hyperinzulinismus citlivý na diazoxid | Hyperinzulinemická hypoglykemie, difuzní forma citlivá na diazoxid |
| uk | Дифузний гіперінсулінізм, чутливий до діазоксиду | Гіперінсулінемічна гіпоглікемія, чутлива до діазоксиду дифузна форма |
| zh | 二氮嗪敏感型弥漫性高胰岛素血症 | 二氮嗪敏感型弥漫性高胰岛素低血糖症 |
| tr | Diazoksite duyarlı yaygın hiperinsülinizm | Hiperinsülinemik hipoglisemi, diazoksit-duyarlı yaygın form |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015624 | E | validated | |
| MONDO | 15624 | E | validated | |
| UMLS | C5679570 | E | validated |
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 (1):
- ORPHA:657Congenital isolated hyperinsulinism
rare inborn errors of metabolism; rare genetic diseases; rare endocrine diseases
Children (9):
- ORPHA:276580Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
- ORPHA:276575Autosomal dominant hyperinsulinism due to SUR1 deficiency
- ORPHA:79299Congenital glucokinase-related hyperinsulinism
- ORPHA:263455Congenital hyperinsulinism due to HNF4A deficiency
- ORPHA:165991Exercise-induced hyperinsulinism
- ORPHA:324575Hyperinsulinism due to HNF1A deficiency
- ORPHA:276556Hyperinsulinism due to UCP2 deficiency
- ORPHA:71212Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
- ORPHA:35878Hyperinsulinism-hyperammonemia syndrome
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/165985
- This record as JSON: /data/d/165985.json