ORPHA:181376
Rare diabetes mellitus type 2
Synonyms: Rare insulin-independent diabetes mellitus
- 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 | Rare diabetes mellitus type 2 | Rare insulin-independent diabetes mellitus |
| fr | Diabète de type 2 rare | Diabète sucré de type 2 rare · Diabète sucré non insulino-dépendant rare |
| de | Seltener Diabetes mellitus Typ 2 | Insulin-unabhängiger Diabetes mellitus, seltene Form |
| es | Diabetes mellitus rara tipo 2 | Diabetes mellitus no insulinodependiente rara |
| it | Diabete mellito raro, tipo 2 | Diabete mellito insulina-indipendente raro |
| nl | Zeldzame diabetes mellitus type 2 | Zeldzame insuline-onafhankelijke diabetes mellitus |
| pt | Diabetes mellitus não insulino-dependente, raros | |
| pl | Rzadka odmiana cukrzycy typu 2 | Rzadka odmiana cukrzycy insulinoniezależnej |
| cs | Vzácný diabetes mellitus 2. typu | Vzácný diabetes mellitus nezávislý na inzulínu |
| uk | Рідкісний цукровий діабет, тип 2 | Рідкісний інсулінонезалежний цукровий діабет |
| zh | 罕见2型糖尿病 | 罕见非胰岛素依赖型糖尿病 |
| tr | Nadir görülen diabetes mellitus tip 2 | Nadir insülin-bağımlı olmayan diabetes mellitus |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15887 | E | validated | |
| UMLS | C5679587 | 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:101952Rare diabetes mellitus
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/181376
- This record as JSON: /data/d/181376.json