Chart 3.8. – Causes of monogenic hypertension.
| Condition | Mode of inheritance | Genes involved |
|---|---|---|
| Liddle's Syndrome | Autosomal dominant | SCNN1B and SCNN1G |
| Congenital adrenal hyperplasia | Autosomal recessive | CYP11B1 |
| Autosomal recessive | CYP17A1 | |
| Apparent mineralocorticoid excess syndrome | Autosomal recessive | HSD11B2 |
| Geller Syndrome | Autosomal dominant | NR3C2 |
| Gordon syndrome (pseudohypoaldosteronism type II) | Autosomal dominant | WNK4 |
| Autosomal dominant | WNK1 | |
| Autosomal recessive or dominant | KLHL3 | |
| Autosomal dominant | CUL3 | |
| Familial hyperaldosteronism type I | Autosomal dominant | CYP11B1 |
| Familial hyperaldosteronism type II | Autosomal dominant | CLCN2 |
| Familial hyperaldosteronism type III | Autosomal dominant | KCNJ5 |
| Familial hyperaldosteronism type IV | Autosomal dominant | CACNA1H |