| Descriptor English: | Fanconi Syndrome | ||||||
| Descriptor Spanish: |
Síndrome de Fanconi
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| Descriptor Portuguese: | Síndrome de Fanconi | ||||||
| Descriptor French: | Syndrome de Fanconi | ||||||
| Entry term(s): |
Adult Fanconi Syndrome Bickel Syndrome, Fanconi De Toni-Debre-Fanconi Syndrome Diabete, Pseudo-Phlorizin Diabetes, Pseudo-Phlorizin Fanconi Bickel Syndrome Fanconi Renotubular Syndrome Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance Fanconi Syndrome without Cystinosis Fanconi Syndrome, Adult Fanconi Syndrome, Renal Fanconi Type Glycogenosis Fanconi-Bickel Syndrome Fanconi-Bickel Syndromes 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 Lignac-Fanconi Syndrome Luder Sheldon Syndrome Luder-Sheldon Syndrome Neonatal De Toni-Debre-Fanconi Syndrome Primary Toni-Debre-Fanconi Syndrome Proximal Renal Tubular Dysfunction Pseudo Phlorizin Diabetes Pseudo-Phlorizin Diabete Pseudo-Phlorizin Diabetes Renal Fanconi Syndrome Renotubular Syndrome, Fanconi Syndrome, Adult Fanconi Syndrome, Fanconi Syndrome, Fanconi Bickel Syndrome, Fanconi Renotubular Syndrome, Fanconi-Bickel Syndrome, Lignac-Fanconi Syndrome, Luder-Sheldon Syndrome, Renal Fanconi Syndromes, Fanconi-Bickel Toni-Debre-Fanconi Syndrome |
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| 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 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D005198 | ||||||
| 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. |
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| Annotation: | do not confuse with other diseases with "FANCONI" as part of the name |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 1965; LIGNAC-FANCONI SYNDROME was LIGNAC-FANCONI DISEASE see METABOLIC DISEASES 1963-1964 |
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| History Note: | 1965; LIGNAC-FANCONI SYNDROME was LIGNAC-FANCONI DISEASE use METABOLIC DISEASES 1963-1964 |
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| Related: |
Glucose Transporter Type 2
MeSH | ||||||
| DeCS ID: | 5302 | ||||||
| Unique ID: | D005198 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1965/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2015/06/22 |
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|
Fanconi Syndrome
- Preferred
Toni-Debre-Fanconi Syndrome
- Related but not broader or narrower
Fanconi Bickel Syndrome
- Narrower
Fanconi Syndrome without Cystinosis
- Narrower
| Concept UI |
M0008225 |
| 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. |
| Preferred term | Fanconi Syndrome |
| Entry term(s) |
Proximal Renal Tubular Dysfunction Syndrome, Fanconi |
| Concept UI |
M0582322 |
| Preferred term | Toni-Debre-Fanconi Syndrome |
| Entry term(s) |
De Toni-Debre-Fanconi Syndrome Idiopathic De Toni-Debre-Fanconi Syndrome Neonatal De Toni-Debre-Fanconi Syndrome Primary Toni-Debre-Fanconi Syndrome |
| Concept UI |
M0582321 |
| Preferred term | Fanconi Bickel Syndrome |
| Entry term(s) |
Bickel Syndrome, Fanconi Diabete, Pseudo-Phlorizin Diabetes, Pseudo-Phlorizin Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance Fanconi Type Glycogenosis Fanconi-Bickel Syndrome Fanconi-Bickel Syndromes 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 Lignac Fanconi Syndrome Lignac-Fanconi Syndrome Pseudo Phlorizin Diabetes Pseudo-Phlorizin Diabete Pseudo-Phlorizin Diabetes Syndrome, Fanconi Bickel Syndrome, Fanconi-Bickel Syndrome, Lignac-Fanconi Syndromes, Fanconi-Bickel |
| Concept UI |
M0532951 |
| Preferred term | Fanconi Syndrome without Cystinosis |
| Entry term(s) |
Adult Fanconi Syndrome Fanconi Renotubular Syndrome Fanconi Syndrome, Adult Fanconi Syndrome, Renal Luder Sheldon Syndrome Luder-Sheldon Syndrome Renal Fanconi Syndrome Renotubular Syndrome, Fanconi Syndrome, Adult Fanconi Syndrome, Fanconi Renotubular Syndrome, Luder-Sheldon Syndrome, Renal Fanconi |
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