ORPHA:181399
Rare hyperthyroidism
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare hyperthyroidism | |
| fr | Hyperthyroïdie rare | |
| de | Hyperthyreose, seltene | |
| es | Hipertiroidismo raro | |
| it | Ipertiroidismo raro | |
| nl | Zeldzame hyperthyreoïdie | |
| pt | Hipertiroidismo raro | |
| pl | Rzadka postać nadczynności tarczycy | |
| cs | Vzácný hypertyreoidismus | |
| uk | Рідкісний гіпертиреоз | |
| zh | 罕见甲状腺功能亢进症 | |
| tr | Nadir hipertiroidi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15894 | E | validated | |
| UMLS | C5680610 | 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 (2):
- ORPHA:183631Rare genetic thyroid disease
rare genetic diseases - ORPHA:101955Rare thyroid 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/181399
- This record as JSON: /data/d/181399.json