ORPHA:95506
Primary hypophysitis
Synonyms: Autoimmune hypophysitis
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Not applicable
- Age of onset
- Adult
- 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 | Primary hypophysitis | Autoimmune hypophysitis |
| fr | Hypophysite primitive | Hypophysite auto-immune |
| de | Hypophysitis, primäre | Hypophysitis, autoimmune |
| es | Hipofisitis primaria | Hipofisitis autoinmune |
| it | Ipofisite primitiva | Ipofisite autoimmune |
| nl | Primaire hypofysitis | Auto-immune hypofysitis |
| pt | Deficiência da hormona pituitária de origem autoimune | |
| pl | Pierwotne zapalenie przysadki | Autoimmunologiczne zapalenie przysadki |
| cs | Primární hypofyzitidy | = en |
| uk | Первинний гіпофізит | Аутоімунний гіпофізит |
| zh | 原发性垂体炎 | 自身免疫性垂体炎 |
| tr | Primer hipofizit | Otoimmün hipofizit |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019835 | E | validated | |
| MeSH | D000069281 | E | validated | |
| UMLS | C0342410 | 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:95502Acquired pituitary hormone deficiency
rare endocrine diseases
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/95506
- This record as JSON: /data/d/95506.json