ORPHA:595337
Adrenal hypoplasia congenita
Synonyms: AHC · Congenital adrenal hypoplasia · Primary adrenal hypoplasia
- Type
- Clinical group
- 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 | Adrenal hypoplasia congenita | AHC · Congenital adrenal hypoplasia · Primary adrenal hypoplasia |
| fr | Hypoplasie congénitale des surrénales | AHC · Hypoplasie congénitale surrénalienne |
| de | Nebennierenhypoplasie, kongenitale | AHC · Kongenitale adrenale Hyperplasie · Nebennierenhypoplasie, primäre |
| es | Hipoplasia suprarrenal congénita | Hipoplasia suprarrenal primaria |
| it | Ipoplasia congenita dei surreni | AHC · Ipoplasia primitiva dei surreni · Ipoplasia surrenalica congenita |
| nl | Congenitale adrenale hypoplasie | AHC · Congenitale bijnierhypoplasie · Congenitale hypoplasie van bijnier · Primaire hypoplasie van bijnier |
| pt | Hipoplasia supra-renal congénita | AHC |
| pl | Wrodzona hipoplazja nadnerczy | Hipoplazja nadnerczy, pierwotna · Hipoplazja nadnerczy, wrodzona |
| cs | Kongenitální adrenální hypoplázie | = en |
| uk | Вроджена гіпоплазія надниркових залоз | AHC · Вроджена гіпоплазія надниркових залоз · Первинна гіпоплазія надниркових залоз |
| zh | Adrenal hypoplasia congenita | = en |
| tr | Adrenal hypoplasia congenita | = en |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C0220766 | E | validated | |
| MedDRA | 10049057 | 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:101960Genetic chronic primary adrenal insufficiency
rare genetic diseases; rare endocrine diseases
Children (6):
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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/595337
- This record as JSON: /data/d/595337.json