ORPHA:443095
Hyperinsulinemic hypoglycaemia
- 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| Lang | Name | Synonyms |
|---|---|---|
| en | Hyperinsulinemic hypoglycaemia | |
| fr | Hypoglycémie hyperinsulinémique | |
| de | Hyperinsulinämische Hypoglykämie | |
| es | Hipoglucemia hiperinsulinémica | |
| it | Ipoglicemia iperinsulinemica | |
| nl | Hyperinsulinemische hypoglycemie | |
| pt | Hipoglicemia hiperinsulinémica | |
| pl | Hipoglikemia hiperinsulinemiczna | |
| cs | Hyperinzulinemická hypoglykémie | |
| uk | Гіперінсулінемічна гіпоглікемія | |
| zh | 高胰岛素所致低血糖症 | |
| tr | Hiperinsülinemik hipoglisemi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0005803 | E | validated | |
| MONDO | 5803 | E | validated | |
| UMLS | C1864903 | E | validated | |
| MedDRA | 10077216 | 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:97978Rare endocrine disease
rare endocrine diseases
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/443095
- This record as JSON: /data/d/443095.json