ORPHA:101960
Genetic 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic chronic primary adrenal insufficiency | |
| fr | Insuffisance surrénale primaire chronique génétique | |
| de | Nebenniereninsuffizienz, chronische primäre, genetisch bedingte | |
| es | Insuficiencia suprarrenal primaria crónica genética | |
| it | Insufficienza surrenale primaria cronica genetica | |
| nl | Genetische chronische primaire adrenale insufficiëntie | Genetische chronische primaire bijnierinsufficiëntie |
| pt | Insuficiência supra-renal primária crónica genética | |
| pl | Genetyczna przewlekła pierwotna niedoczynność nadnerczy | |
| cs | Geneticky podmíněné chronické primární adrenální insuficience | |
| uk | Генетично обумовлена хронічна первинна надниркова недостатність | |
| zh | 遗传性慢性原发性肾上腺功能不全 | |
| tr | Genetik kronik primer adrenal yetmezlik |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681791 | E | validated | |
| GARD | 19804 | 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 (2):
- ORPHA:101959Chronic primary adrenal insufficiency
rare endocrine diseases - ORPHA:183637Rare genetic adrenal disease
rare genetic diseases
Children (11):
- ORPHA:16855846,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency
- ORPHA:595337Adrenal hypoplasia congenita
- ORPHA:977Adrenomyodystrophy
- ORPHA:3453Autoimmune polyendocrinopathy type 1
- ORPHA:418Congenital adrenal hyperplasia
- ORPHA:199332Endocrine-cerebro-osteodysplasia syndrome
- ORPHA:361Familial glucocorticoid deficiency
- ORPHA:289548Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
- ORPHA:44Neonatal adrenoleukodystrophy
- ORPHA:869Triple A syndrome
- ORPHA:43X-linked adrenoleukodystrophy
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/101960
- This record as JSON: /data/d/101960.json