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Fanconis syndrom
Hierarki: | ∟ ∟ ∟ ∟ ∟ Fanconis syndrom 34 sidobegrepp∟ ∟ ∟ ∟ Fanconis syndrom 34 sidobegrepp∟ ∟ ∟ ∟ ∟ Fanconis syndrom 34 sidobegrepp∟ ∟ ∟ ∟ ∟ Fanconis syndrom 34 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ Fanconis syndrom 34 sidobegrepp∟ ∟ ∟ ∟ ∟ Fanconis syndrom 34 sidobegreppX |
Bredare villkor: | ∟ ∟ ∟ ∟ ∟ Fanconis syndrom ∟ ∟ ∟ ∟ Fanconis syndrom ∟ ∟ ∟ ∟ ∟ Fanconis syndrom ∟ ∟ ∟ ∟ ∟ Fanconis syndrom ∟ ∟ ∟ ∟ ∟ ∟ Fanconis syndrom ∟ ∟ ∟ ∟ ∟ Fanconis syndrom |
Anmärkning: | 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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historyNote*: | 65; LIGNAC-FANCONI SYNDROME was LIGNAC-FANCONI DISEASE see under METABOLIC DISEASES 1963-64
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publicMeSHNote*: | 65; LIGNAC-FANCONI SYNDROME was LIGNAC-FANCONI DISEASE see under METABOLIC DISEASES 1963-64
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activeMeSHYear*: | 2007X |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1965-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | NLMX |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Fanconin oireyhtymä (fi) XFanconin syndrooma (fi, ersatt) Fanconi Syndrome (en) Renal Fanconi Syndrome (en, ersatt) Proximal Renal Tubular Dysfunction (en, ersatt) Fanconi Renotubular Syndrome (en, ersatt) Lignac-Fanconi Syndrome (en, ersatt) De Toni-Debre-Fanconi Syndrome (en, ersatt) Syndroma Fanconi (la-FI, ersatt) |
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