ORPHA:178045
Transient congenital hypothyroidism
- 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 | Transient congenital hypothyroidism | |
| fr | Hypothyroïdie congénitale transitoire | |
| de | Hypothyreose, kongenitale transiente | |
| es | Hipotiroidismo congénito transitorio | |
| it | Ipotiroidismo congenito transitorio | |
| nl | Voorbijgaande congenitale hypothyreoïdie | |
| pt | Hipotiroidismo congénito transitório | |
| pl | Wrodzona przejmijająca niedoczynność tarczycy | |
| cs | Přechodná vrozená hypotyreóza | |
| uk | Транзиторний вроджений гіпотиреоз | |
| zh | 暂时性先天性甲状腺功能减退症 | |
| tr | Geçici doğumsal hipotiroidi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5A00.03 | E | specific | validated |
| MONDO | 0015792 | E | validated | |
| MONDO | 15792 | 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:442Congenital hypothyroidism
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/178045
- This record as JSON: /data/d/178045.json