ORPHA:101955
Rare 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare thyroid disease | |
| fr | Maladie rare de la thyroïde | |
| de | Schilddrüsenkrankheit, seltene | |
| es | Enfermedad rara de la tiroides | |
| it | Malattia tiroidea rara | |
| nl | Zeldzame schildklierziekte | |
| pt | Doença da tiroide rara | |
| pl | Rzadkie choroby tarczycy | |
| cs | Vzácné tyreoidální onemocnění | |
| uk | Рідкісні захворювання щитовидної залози | |
| zh | 罕见甲状腺疾病 | |
| tr | Nadir tiroid hastalığı |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15125 | E | validated | |
| UMLS | C5681800 | E | validated | |
| GARD | 19799 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:97978Rare endocrine disease
rare endocrine diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:872OBSOLETE: Disorder in the hormonal synthesis with or without goiter referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/101955
- This record as JSON: /data/d/101955.json