| hypertensie door 'gain-of-function'-mutatie in mineralocorticoïdreceptor (aandoening) | | hypertensie door 'gain-of-function'-mutatie in mineralocorticoïdreceptor | | Hypertension due to gain-of-function mutation in mineralocorticoid receptor | | Pseudohyperaldosteronism type 2
Early-onset hypertension with exacerbation in pregnancy
| | A rare genetic cause of hypertension characterized by severe early-onset therapy-resistant hypertension due to a gain-of-function mutation in the mineralocorticoid receptor. The condition is associated with suppressed plasma renin activity and low serum aldosterone levels and is markedly exacerbated during pregnancy. |
| | Id | 766937004 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | I15.1 | | Term | Hypertensie secundair aan andere nieraandoeningen |
|
| SNOMED CT to Orphanet simple map | 88660 |
| SNOMED CT to ICD-10 extended map | | Target | I15.1 | | Rule | TRUE | | Advice | ALWAYS I15.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|
