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
Early-onset hypertension with exacerbation in pregnancy
Pseudohyperaldosteronism type 2
A rare genetic hypertension with characteristics of a familial severe hypertension with an onset before age 20 years, associated with suppressed plasma renin and low aldosterone levels in the presence of low or normal levels of the mineralocorticoid aldosterone, that is highly resistant to antihypertensive medication. During pregnancy, there is a marked exacerbation of hypertension, accompanied by low serum potassium levels and undetectable aldosterone levels, but without signs of preeclampsia, requiring early delivery.
Has interpretationverhoogd
referentieset met complexe 'mapping' naar ICD-10
AdviceALWAYS I15.1
CorrelationSNOMED CT source code to target map code correlation not specified