| alternative label
| - Pseudo-hypoaldostéronisme
- Pseudohypoaldosteronism Type 1, Autosomal Recessive
- Pseudohypoaldosteronism, Type II
- Pseudohypoaldostéronisme de type 1
- Familial Hypertensive Hyperkalemias
- HHF (Hypertension Hyperkaliémique Familiale)
- Hyperpotassemia and Hypertension, Familial
- Hypertension hyperkaliémique familiale
- PHA1 (PseudoHypoAldostéronisme de type 1)
- Pseudohypoaldosteronism Type 1
- Pseudohypoaldosteronism Type II
- Pseudohypoaldosteronism, Type I
- Syndrome, Gordon Hyperkalemia-Hypertension
- Type I Pseudohypoaldosteronism
- Familial Hypertensive Hyperkalemia
- Hypertensive Hyperkalemia, Familial
- PHA (PseudoHypoAldostéronisme)
- Pseudohypoaldosteronism
- Pseudohypoaldosteronism Type I
- Pseudohypoaldosteronisms
- Type II Pseudohypoaldosteronisms
- Type II, Pseudohypoaldosteronism
- Pseudohypoaldostéronisme de type 1 autosomique dominant
- Pseudohypoaldostéronisme de type 1 autosomique récessif
- Pseudohypoaldosteronism, Type I, Autosomal Recessive
- Familial Hyperpotassemia and Hypertension
- Gordon Hyperkalemia-Hypertension Syndrome
- Hyperkalemia-Hypertension Syndrome, Gordon
- Hyperkalemias, Familial Hypertensive
- Pseudohypoaldosteronism Type 2s
- Pseudohypoaldosteronisms, Type I
- Pseudohypoaldosteronisms, Type II
- Pseudohypoaldostéronisme de type 2
- Syndrome de Gordon
- Type Is, Pseudohypoaldosteronism
- Hyperkalemia, Familial Hypertensive
- Hypertensive Hyperkalemias, Familial
- Pseudohypoaldosteronism Type 1, Autosomal Dominant
- Pseudohypoaldosteronism Type 1s
- Pseudohypoaldosteronism Type 2
- Syndrome d'hyperkaliémie familiale
- Type I, Pseudohypoaldosteronism
- Pseudohypoaldosteronism, Type I, Autosomal Dominant
- Gordon Hyperkalemia Hypertension Syndrome
- PHA2 (PseudoHypoAldostéronisme de type 2)
- Pseudohypoaldosteronism Type IIs
- Pseudohypoaldosteronism Type Is
- Type 1, Pseudohypoaldosteronism
- Type II Pseudohypoaldosteronism
- Type IIs, Pseudohypoaldosteronism
|
| note
| - Autosomal dominant syndrome of renal electrolyte transport dysfunctions. The clinical features include salt-sensitive hypertension, renal HYPERKALEMIA without sodium wasting, normal glomerular filtration rate and metabolic acidosis (hyperchloremic acidemia and HYPERCALCIURIA). Wnk1 and Wnk4 mutations are responsible for the disorder
- A heterogeneous group of disorders characterized by renal electrolyte transport dysfunctions. Congenital forms are rare autosomal disorders characterized by neonatal hypertension, HYPERKALEMIA, increased RENIN activity and ALDOSTERONE concentration. The Type I features HYPERKALEMIA with sodium wasting; Type II, HYPERKALEMIA without sodium wasting. Pseudohypoaldosteronism can be the result of a defective renal electrolyte transport protein or acquired after KIDNEY TRANSPLANTATION
- Rare autosomal disorder of renal electrolyte transport dysfunctions. The Type I features HYPERKALEMIA with sodium wasting; Type II, HYPERKALEMIA without sodium wasting. Loss of function mutations in EPITHELIAL SODIUM CHANNELS subunits (autosomal dominant) or MINERALOCORTICOID RECEPTORS (autosomal recessive) cause the disorder. Different mutations in EPITHELIAL SODIUM CHANNELS subunits cause Liddle syndrome
|
![[RDF Data]](/fct/images/sw-rdf-blue.png)
