ORPHA:101963
Acquired chronic primary adrenal insufficiency
- 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 | Acquired chronic primary adrenal insufficiency | |
| fr | Insuffisance surrénale primaire chronique acquise | |
| de | Nebenniereninsuffizienz, chronische primäre, erworbene | |
| es | Insuficiencia suprarrenal primaria crónica adquirida | |
| it | Insufficienza surrenale primaria cronica acquisita | |
| nl | Verworven chronische primaire adrenale insufficiëntie | |
| pt | Insuficiência supra-renal primária crónica adquirida | |
| pl | Nabyta przewlekła pierwotna niedoczynność nadnerczy | |
| cs | Získané chronické primární adrenální insuficience | |
| uk | Набута хронічна первинна надниркова недостатність | |
| zh | 获得性慢性原发性肾上腺功能不全 | |
| tr | Edinsel kronik primer adrenal yetmezlik |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15130 | E | validated | |
| UMLS | C5681792 | 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:101959Chronic primary adrenal insufficiency
rare endocrine diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:95701OBSOLETE: Congenital adrenal hypoplasia of maternal cause 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/101963
- This record as JSON: /data/d/101963.json