Pseudohypoaldosteronism [pseudohypoaldosteronismus]

topical
10
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

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 1
CO
complications
CN
congenital 1
DI
diagnosis 6
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 3
GE
genetics 3
HI
history
IM
immunology
ME
metabolism 1
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 1
PP
physiopathology 2
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 1
UR
urine 1
VE
veterinary
VI
virology

C Diseases
C12 Urogenital Diseases 8
C12.050 Female Urogenital Diseases and Pregnancy Complications 132
C12.050.351 Female Urogenital Diseases 153
C12.050.351.968 Urologic Diseases 836
C12.050.351.968.419 Kidney Diseases 3 067
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 20
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 18
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 10
C12.050.351.968.419.815.885 Renal Aminoacidurias 27
C12.200 Male Urogenital Diseases 200
C12.200.777 Urologic Diseases 836
C12.200.777.419 Kidney Diseases 3 067
C12.200.777.419.815 Renal Tubular Transport, Inborn Errors 36
C12.200.777.419.815.093 Acidosis, Renal Tubular 59
C12.200.777.419.815.279 Bartter Syndrome 20
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 18
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 10
C12.200.777.419.815.885 Renal Aminoacidurias 27
C12.950 Urologic Diseases 836
C12.950.419 Kidney Diseases 3 067
C12.950.419.815 Renal Tubular Transport, Inborn Errors 36
C12.950.419.815.093 Acidosis, Renal Tubular 59
C12.950.419.815.279 Bartter Syndrome 20
C12.950.419.815.364 Dent Disease 1
C12.950.419.815.450 Fanconi Syndrome 23
C12.950.419.815.491 Gitelman Syndrome 18
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 10
C12.950.419.815.885 Renal Aminoacidurias 27
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 215
C16.320.831 Renal Tubular Transport, Inborn Errors 36
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 18
C16.320.831.532 Glycosuria, Renal 36
C16.320.831.647 Hypophosphatemia, Familial 12
C16.320.831.698 Liddle Syndrome 4
C16.320.831.750 Oculocerebrorenal Syndrome 9
C16.320.831.770 Pseudohypoaldosteronism 10
C16.320.831.885 Renal Aminoacidurias 27

Pseudohypoaldosteronism, Type IIa Disease MeSH Browser

Pseudohypoaldosteronism, Type IIb Disease MeSH Browser

Pseudohypoaldosteronism, Type IIc Disease MeSH Browser

Tunglang Savage Bellman syndrome Disease MeSH Browser

Back Add