ORPHA:183628
Rare genetic hypothalamic or pituitary 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 hypothalamic or pituitary disease | |
| fr | Maladie hypophysaire ou hypothalamique rare d'origine génétique | |
| de | Hypothalamus- oder Hypophysenkrankheit, genetisch bedingte, seltene | |
| es | Enfermedad hipofisaria o hipotalámica rara de origen genético | |
| it | Malattia genetica rara dell'ipotalamo e dell'ipofisi | |
| nl | Zeldzame genetische hypothalamische of hypofysaire ziekte | |
| pt | Doença genética hipotalâmica ou pituitária rara | |
| pl | Rzadka genetyczna choroba przysadki lub podwzgórza | |
| cs | Vzácné dědičné onemocnění hypotalamu nebo hypofýzy | |
| uk | Рідкісні генетично обумовлені захворювання гіпоталамуса або гіпофіза | |
| zh | 罕见遗传性下丘脑或垂体疾病 | |
| tr | Nadir genetik hipotalamik veya hipofiz hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15968 | E | validated | |
| UMLS | C5680536 | 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/183628
- This record as JSON: /data/d/183628.json