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Descriptor en español: |
Síndrome de Fanconi
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Descriptor en inglés: | Fanconi Syndrome | ||||||
Descriptor en portugués: | Síndrome de Fanconi | ||||||
Descriptor en francés: | Syndrome de Fanconi | ||||||
Término(s) alternativo(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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Código(s) jeráquico(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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Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D005198 | ||||||
Nota de alcance: | 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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Nota de indización: | do not confuse with other diseases with "FANCONI" as part of the name |
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Calificadores permitidos: |
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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Nota Pública de MeSH: | 1965; LIGNAC-FANCONI SYNDROME was LIGNAC-FANCONI DISEASE see METABOLIC DISEASES 1963-1964 |
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Nota de historia: | 1965; LIGNAC-FANCONI SYNDROME was LIGNAC-FANCONI DISEASE use METABOLIC DISEASES 1963-1964 |
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Vea también los descriptores: |
Glucose Transporter Type 2
MeSH | ||||||
Identificador de DeCS: | 5302 | ||||||
ID del Descriptor: | D005198 | ||||||
Documentos indizados en la Biblioteca Virtual de Salud (BVS): | Haga clic aquí para acceder a los documentos de la BVS | ||||||
Fecha de establecimiento: | 01/01/1965 | ||||||
Fecha de entrada: | 01/01/1999 | ||||||
Fecha de revisión: | 22/06/2015 |
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Fanconi Syndrome
- Concepto preferido
Toni-Debre-Fanconi Syndrome
- Relacionado pero no más amplio ni más estrecho
Fanconi Bickel Syndrome
- Más estrecho
Fanconi Syndrome without Cystinosis
- Más estrecho
UI del concepto |
M0008225 |
Nota de alcance | 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. |
Término preferido | Fanconi Syndrome |
Término(s) alternativo(s) |
Proximal Renal Tubular Dysfunction Syndrome, Fanconi |
UI del concepto |
M0582322 |
Término preferido | Toni-Debre-Fanconi Syndrome |
Término(s) alternativo(s) |
De Toni-Debre-Fanconi Syndrome Idiopathic De Toni-Debre-Fanconi Syndrome Neonatal De Toni-Debre-Fanconi Syndrome Primary Toni-Debre-Fanconi Syndrome |
UI del concepto |
M0582321 |
Término preferido | Fanconi Bickel Syndrome |
Término(s) alternativo(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 |
UI del concepto |
M0532951 |
Término preferido | Fanconi Syndrome without Cystinosis |
Término(s) alternativo(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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