Fanconi Syndrome [Fanconiho syndrom]

topical
23
Terms

Debréův-De Toniho-Fanconiho syndrom
Fanconiho-Bickelův syndrom
Lignacův-Fanconiho syndrom
Luderův-Sheldonův syndrom
renální Fanconiho syndrom
syndrom Luderův-Sheldonův

 

Adult Fanconi Syndrome
De Toni-Debre-Fanconi Syndrome
Fanconi Bickel Syndrome
Fanconi Renotubular Syndrome
Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance
Fanconi Syndrome without Cystinosis
Fanconi-Bickel Syndrome
Glycogen Storage Disease XI
Glycogenosis, Fanconi Type
Hepatic Glycogenosis with Amino Aciduria and Glucosuria
Hepatic Glycogenosis with Fanconi Nephropathy
Hepatorenal Glycogenosis with Renal Fanconi Syndrome
Idiopathic De Toni-Debre-Fanconi Syndrome
Lignac-Fanconi Syndrome
Luder-Sheldon Syndrome
Neonatal De Toni-Debre-Fanconi Syndrome
Primary Toni-Debre-Fanconi Syndrome
Proximal Renal Tubular Dysfunction
Pseudo-Phlorizin Diabetes
Renal Fanconi Syndrome
Toni-Debre-Fanconi Syndrome

Persistent link   https://www.medvik.cz/link/D005198
Definition

A hereditary or acquired form of generalized dysfunction of the PROXIMAL KIDNEY TUBULE without primary involvement of the KIDNEY GLOMERULUS. It is usually characterized by the tubular wasting of nutrients and salts (GLUCOSE; AMINO ACIDS; PHOSPHATES; and BICARBONATES) resulting in HYPOKALEMIA; ACIDOSIS; HYPERCALCIURIA; and PROTEINURIA.

Annotation
do not confuse with other diseases with "FANCONI" as part of the name
DUI
D005198 MeSH Browser
CUI
M0008225
History note
1965; LIGNAC-FANCONI SYNDROME was LIGNAC-FANCONI DISEASE use METABOLIC DISEASES 1963-1964
Public note
1965; LIGNAC-FANCONI SYNDROME was LIGNAC-FANCONI DISEASE see METABOLIC DISEASES 1963-1964

C Diseases
C12.050.351.968 Urologic Diseases 834
C12.050.351.968.419 Kidney Diseases 3 060
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 3 060
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 3 060
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

Deal Barratt Dillon syndrome Disease MeSH Browser

Preeyasombat Varavithya syndrome Disease MeSH Browser

Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction Disease MeSH Browser