| familiair hyperaldosteronisme type 1 (aandoening) | | familiair hyperaldosteronisme type 1 | | Familial hyperaldosteronism type 1 | | Glucocorticoid-sensitive hypertension
Familial hyperaldosteronism type I
Dexamethasone-sensitive hypertension
Glucocorticoid-suppressible hyperaldosteronism
GRA - glucocorticoid-remediable aldosteronism
Glucocorticoid-remediable aldosteronism
| | A rare inherited disorder due to the ectopic expression of the aldosterone synthase in the fascicular zone of the adrenal gland and marked with early severe hypertension (often occurring before the age of 20), biological signs of primary aldosteronism of variable intensity, and an abnormal elevated level of 18-oxo- and 18-hydroxycortisol. |
| | Id | 703232003 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E26.0 | | Term | Primair hyperaldosteronisme |
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| SNOMED CT to Orphanet simple map | 403 |
| SNOMED CT to ICD-10 extended map | | Target | E26.0 | | Rule | TRUE | | Advice | ALWAYS E26.0 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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