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Fanconi Syndrome MeSH Descriptor Data 2023


MeSH Heading
Fanconi Syndrome
Tree Number(s)
C12.050.351.968.419.815.450
C12.200.777.419.815.450
C12.950.419.815.450
C16.320.831.450
Unique ID
D005198
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D005198
Annotation
do not confuse with other diseases with "FANCONI" as part of the name
Scope Note
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.
Entry Term(s)
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
See Also
Glucose Transporter Type 2
Public MeSH Note
1965; LIGNAC-FANCONI SYNDROME was LIGNAC-FANCONI DISEASE see METABOLIC DISEASES 1963-1964
History Note
1965; LIGNAC-FANCONI SYNDROME was LIGNAC-FANCONI DISEASE use METABOLIC DISEASES 1963-1964
Date Established
1965/01/01
Date of Entry
1999/01/01
Revision Date
2021/06/30
Fanconi Syndrome Preferred
Toni-Debre-Fanconi Syndrome Related
Fanconi Bickel Syndrome Narrower
Fanconi Syndrome without Cystinosis Narrower
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