ORPHA:95502
Acquired pituitary hormone deficiency
- 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 | Acquired pituitary hormone deficiency | |
| fr | Insuffisance hypophysaire acquise | |
| de | Hypophysenhormon-Mangel, erworbener | |
| es | Deficiencia adquirida de hormonas hipofisarias | |
| it | Deficit acquisito degli ormoni pituitari | |
| nl | Verworven hypofysehormoondeficiëntie | |
| pt | Deficiência de hormona pituitária adquirida | |
| pl | Nabyty Niedobór hormonów przysadki | |
| cs | Získaný deficit hypofyzárních hormonů | |
| uk | Набутий дефіцит гормонів гіпофіза | |
| zh | 获得性垂体激素缺乏症 | |
| tr | Edinsel hipofiz hormonu eksikliği |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019832 | E | validated | |
| UMLS | C5681569 | 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:101957Pituitary deficiency
rare endocrine diseases
Children (10):
- ORPHA:641350Immunotherapy induced hypophysitis
- ORPHA:199299Late-onset isolated ACTH deficiency
- ORPHA:95613Pituitary apoplexy
- ORPHA:95505Pituitary hormone deficiency of meningeal origin
- ORPHA:95503Pituitary hormone deficiency of tumoral origin
- ORPHA:95611Pituitary hormone deficiency of vascular origin
- ORPHA:95617Pituitary hormone deficiency secondary to a granulomatous disease
- ORPHA:95618Pituitary hormone deficiency secondary to storage disease
- ORPHA:95619Post-traumatic pituitary deficiency
- ORPHA:95506Primary hypophysitis
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/95502
- This record as JSON: /data/d/95502.json