ORPHA:183631
Rare genetic thyroid disease
- 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 genetic thyroid disease | |
| fr | Maladie rare de la thyroïde d'origine génétique | |
| de | Schilddrüsenkrankheit, genetisch bedingte, seltene | |
| es | Enfermedad rara de la tiroides de origen genético | |
| it | Malattia genetica rara della tiroide | |
| nl | Zeldzame genetische schildklierziekte | |
| pt | Doença da tiroide genética rara | |
| pl | Rzadka genetyczna choroba tarczycy | |
| cs | Vzácná geneticky podmíněná onemocnění štítné žlázy | |
| uk | Рідкісне генетично обумовлене захворювання щитовидної залози | |
| zh | 罕见遗传性甲状腺疾病 | |
| tr | Nadir genetik tiroid hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15969 | E | validated | |
| UMLS | C5680539 | 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:156638Rare genetic endocrine disease
rare genetic 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/183631
- This record as JSON: /data/d/183631.json