ORPHA:95611
Pituitary hormone deficiency of vascular origin
- 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 | Pituitary hormone deficiency of vascular origin | |
| fr | Insuffisance hypophysaire d'origine vasculaire | |
| de | Hypophysenhormon-Mangel mit vaskulärem Ursprung | |
| es | Deficiencia de la hormona hipofisaria de origen vascular | |
| it | Deficit degli ormoni pituitari di origine vascolare | |
| nl | Hypofysehormoondeficiëntie van vasculaire oorsprong | |
| pt | Deficiência de hormona pituitária de origem vascular | |
| pl | Niedobór hormonów przysadki pochodzenia naczyniowego | |
| cs | Deficit hypofyzárních hormonů cévního původu | |
| uk | Дефіцит гормонів гіпофіза судинного походження | |
| zh | 血管源性垂体激素缺乏症 | |
| tr | Damar kökenli hipofiz hormonu eksikliği |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681571 | 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:95502Acquired pituitary hormone deficiency
rare endocrine diseases
Children (1):
Codes that Orphanet moved or referred to this one:
- ORPHA:95615OBSOLETE: Pituitary deficiency secondary to an anevrysm referred to · inactive
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/95611
- This record as JSON: /data/d/95611.json