Acidosis, Renal Tubular [renální tubulární acidóza]

topical
59
Terms

acidóza renální tubulární
distální RTA
proximální RTA
renální tubulární acidóza distálního typu
renální tubulární acidóza typu I
renální tubulární acidóza typu II
renální tubulární acidóza, typ I
renální tubulární acidóza, typ II
RTA

 

Acidosis, Renal Tubular, Type I
Acidosis, Renal Tubular, Type II
Autosomal Dominant Distal Renal Tubular Acidosis
Classic Distal Renal Tubular Acidosis
Distal Renal Tubular Acidosis
Proximal Renal Tubular Acidosis
Renal Tubular Acidosis
Renal Tubular Acidosis 1
Renal Tubular Acidosis I
Renal Tubular Acidosis II
Renal Tubular Acidosis, Distal, Autosomal Dominant
Renal Tubular Acidosis, Proximal
Renal Tubular Acidosis, Proximal, with Ocular Abnormalities
Renal Tubular Acidosis, Type I
Renal Tubular Acidosis, Type II
RTA, Classic Type
RTA, Distal Type, Autosomal Dominant
RTA, Gradient Type
RTA, Proximal Type
Type I Renal Tubular Acidosis
Type II Renal Tubular Acidosis

Persistent link   https://www.medvik.cz/link/D000141
Definition

A group of genetic disorders of the KIDNEY TUBULES characterized by the accumulation of metabolically produced acids with elevated plasma chloride, hyperchloremic metabolic ACIDOSIS. Defective renal acidification of URINE (proximal tubules) or low renal acid excretion (distal tubules) can lead to complications such as HYPOKALEMIA, hypercalcinuria with NEPHROLITHIASIS and NEPHROCALCINOSIS, and RICKETS.

DUI
D000141 MeSH Browser
CUI
M0000215
History note
65
Public note
65

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced 1
CL
classification 2
CO
complications 11
CN
congenital
DI
diagnosis 25
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 6
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 15
GE
genetics 7
HI
history
IM
immunology
ME
metabolism 4
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 5
PP
physiopathology 6
PC
prevention & control 1
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 12
UR
urine 3
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
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 200
C18.452.076 Acid-Base Imbalance 288
C18.452.076.176 Acidosis 319
C18.452.076.176.180 Acidosis, Lactic 119
C18.452.076.176.210 Acidosis, Renal Tubular 59
C18.452.076.176.310 Acidosis, Respiratory 40
C18.452.076.176.652 Ketosis 32

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