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.

Descriptor ID	D011546
MeSH Number(s)	C12.777.419.815.770 C13.351.968.419.815.770 C16.320.565.861.770 C18.452.648.861.770
Concept/Terms	Pseudohypoaldosteronism Pseudohypoaldosteronism Pseudohypoaldosteronisms Pseudohypoaldosteronism, Type I Pseudohypoaldosteronism, Type I Pseudohypoaldosteronisms, Type I Type I Pseudohypoaldosteronism Pseudohypoaldosteronism Type 1 Pseudohypoaldosteronism Type 1s Type 1, Pseudohypoaldosteronism Pseudohypoaldosteronism Type I Pseudohypoaldosteronism Type Is Type I, Pseudohypoaldosteronism Type Is, Pseudohypoaldosteronism Pseudohypoaldosteronism, Type II Pseudohypoaldosteronism, Type II Pseudohypoaldosteronisms, Type II Type II Pseudohypoaldosteronism Type II Pseudohypoaldosteronisms Gordon Hyperkalemia-Hypertension Syndrome Gordon Hyperkalemia Hypertension Syndrome Hyperkalemia-Hypertension Syndrome, Gordon Syndrome, Gordon Hyperkalemia-Hypertension Pseudohypoaldosteronism Type 2 Pseudohypoaldosteronism Type 2s Pseudohypoaldosteronism Type II Pseudohypoaldosteronism Type IIs Type II, Pseudohypoaldosteronism Type IIs, Pseudohypoaldosteronism Pseudohypoaldosteronism, Type I, Autosomal Recessive Pseudohypoaldosteronism, Type I, Autosomal Recessive Pseudohypoaldosteronism Type 1, Autosomal Recessive Hyperpotassemia and Hypertension, Familial Hyperpotassemia and Hypertension, Familial Familial Hyperpotassemia and Hypertension Familial Hypertensive Hyperkalemia Hypertensive Hyperkalemia, Familial Familial Hypertensive Hyperkalemias Hyperkalemia, Familial Hypertensive Hyperkalemias, Familial Hypertensive Hypertensive Hyperkalemias, Familial Pseudohypoaldosteronism, Type I, Autosomal Dominant Pseudohypoaldosteronism, Type I, Autosomal Dominant Pseudohypoaldosteronism Type 1, Autosomal Dominant

Below are MeSH descriptors whose meaning is more general than "Pseudohypoaldosteronism".

Below are MeSH descriptors whose meaning is related to "Pseudohypoaldosteronism".

Below are MeSH descriptors whose meaning is more specific than "Pseudohypoaldosteronism".