Pseudohypoaldosteronism [pseudohypoaldosteronismus]

topical
9
Terms

familiární hyperkalemie a hypertenze
Gordonův syndrom
pseudohypoaldosteronismus typu 1
pseudohypoaldosteronismus typu 2
pseudohypoaldosteronismus typu I
pseudohypoaldosteronismus typu I, autozomálně dominantní
pseudohypoaldosteronismus typu I, autozomálně recesivní
pseudohypoaldosteronismus typu II

 

Familial Hyperpotassemia and Hypertension
Familial Hypertensive Hyperkalemia
Gordon Hyperkalemia-Hypertension Syndrome
Hyperpotassemia and Hypertension, Familial
Hypertensive Hyperkalemia, Familial
Pseudohypoaldosteronism Type 1
Pseudohypoaldosteronism Type 1, Autosomal Dominant
Pseudohypoaldosteronism Type 1, Autosomal Recessive
Pseudohypoaldosteronism Type 2
Pseudohypoaldosteronism Type I
Pseudohypoaldosteronism Type II
Pseudohypoaldosteronism, Type I
Pseudohypoaldosteronism, Type I, Autosomal Dominant
Pseudohypoaldosteronism, Type I, Autosomal Recessive
Pseudohypoaldosteronism, Type II

Persistent link   https://www.medvik.cz/link/D011546
Definition

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.

DUI
D011546 MeSH Browser
CUI
M0017948
Previous indexing
Aldosterone (1971-1987); Hyperaldosteronism (1975-1980); Renal Tubular Transport, Inborn Errors (1971-1987)
History note
1991(1988); use RENAL TUBULAR TRANSPORT, INBORN ERRORS 1988-90
Public note
1991; see RENAL TUBULAR TRANSPORT, INBORN ERRORS 1988-90

C Diseases
C12.050.351.968 Urologic Diseases 834
C12.050.351.968.419 Kidney Diseases 3 059
C12.050.351.968.419.815 Renal Tubular Transport, Inborn Errors 36
C12.050.351.968.419.815.093 Acidosis, Renal Tubular 59
C12.050.351.968.419.815.279 Bartter Syndrome 19
C12.050.351.968.419.815.364 Dent Disease 1
C12.050.351.968.419.815.450 Fanconi Syndrome 23
C12.050.351.968.419.815.491 Gitelman Syndrome 17
C12.050.351.968.419.815.532 Glycosuria, Renal 36
C12.050.351.968.419.815.647 Hypophosphatemia, Familial 12
C12.050.351.968.419.815.683 Liddle Syndrome 4
C12.050.351.968.419.815.720 Oculocerebrorenal Syndrome 9
C12.050.351.968.419.815.770 Pseudohypoaldosteronism 9
C12.050.351.968.419.815.885 Renal Aminoacidurias 27
C12.200.777 Urologic Diseases 834
C12.200.777.419 Kidney Diseases 3 059
C12.200.777.419.815.093 Acidosis, Renal Tubular 59
C12.200.777.419.815.279 Bartter Syndrome 19
C12.200.777.419.815.364 Dent Disease 1
C12.200.777.419.815.450 Fanconi Syndrome 23
C12.200.777.419.815.491 Gitelman Syndrome 17
C12.200.777.419.815.532 Glycosuria, Renal 36
C12.200.777.419.815.647 Hypophosphatemia, Familial 12
C12.200.777.419.815.683 Liddle Syndrome 4
C12.200.777.419.815.720 Oculocerebrorenal Syndrome 9
C12.200.777.419.815.770 Pseudohypoaldosteronism 9
C12.200.777.419.815.885 Renal Aminoacidurias 27
C12.950.419 Kidney Diseases 3 059
C12.950.419.815.093 Acidosis, Renal Tubular 59
C12.950.419.815.279 Bartter Syndrome 19
C12.950.419.815.364 Dent Disease 1
C12.950.419.815.450 Fanconi Syndrome 23
C12.950.419.815.491 Gitelman Syndrome 17
C12.950.419.815.532 Glycosuria, Renal 36
C12.950.419.815.647 Hypophosphatemia, Familial 12
C12.950.419.815.683 Liddle Syndrome 4
C12.950.419.815.720 Oculocerebrorenal Syndrome 9
C12.950.419.815.770 Pseudohypoaldosteronism 9
C12.950.419.815.885 Renal Aminoacidurias 27
C16.320.831.093 Acidosis, Renal Tubular 59
C16.320.831.271 Dent Disease 1
C16.320.831.450 Fanconi Syndrome 23
C16.320.831.491 Gitelman Syndrome 17
C16.320.831.532 Glycosuria, Renal 36
C16.320.831.647 Hypophosphatemia, Familial 12
C16.320.831.698 Liddle Syndrome 4
C16.320.831.770 Pseudohypoaldosteronism 9
C16.320.831.885 Renal Aminoacidurias 27