ORPHA:183637
Rare genetic adrenal disease
- 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 | Rare genetic adrenal disease | |
| fr | Maladie génétique rare des surrénales | |
| de | Nebennierenkrankheit, genetisch bedingte, seltene | |
| es | Enfermedad suprarrenal rara de origen genético | |
| it | Malattia genetica rara dei surreni | |
| nl | Zeldzame genetische adrenale ziekte | Zeldzame genetische bijnierziekte |
| pt | Doença supra-renal genética rara | |
| pl | Rzadka genetyczna choroba nadnerczy | |
| cs | Vzácné dědičné choroby nadledvin | |
| uk | Рідкісне генетично обумовлене захворювання надниркових залоз | |
| zh | 罕见遗传性肾上腺疾病 | |
| tr | Nadir genetik adrenal hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15971 | E | validated | |
| UMLS | C5680534 | 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:156638Rare genetic endocrine disease
rare genetic diseases
Children (10):
- ORPHA:181412Adrenogenital syndrome
- ORPHA:320Apparent mineralocorticoid excess
- ORPHA:199247Corticosteroid-binding globulin deficiency
- ORPHA:189427Cushing syndrome due to bilateral macronodular adrenocortical disease
- ORPHA:324299EPAS1-related polycythemia-pheochromocytoma/paraganglioma syndrome
- ORPHA:427Familial hypoaldosteronism
- ORPHA:101960Genetic chronic primary adrenal insufficiency
- ORPHA:371861Genetic hyperaldosteronism
- ORPHA:29072Hereditary pheochromocytoma-paraganglioma
- ORPHA:2976Pseudoleprechaunism syndrome, Patterson type
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/183637
- This record as JSON: /data/d/183637.json