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Fanconi Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Fanconi Syndrome 34 coordinate concepts∟ ∟ ∟ ∟ ∟ Fanconi Syndrome 34 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Fanconi Syndrome 34 coordinate concepts∟ ∟ ∟ ∟ Fanconi Syndrome 34 coordinate concepts∟ ∟ ∟ ∟ ∟ Fanconi Syndrome 34 coordinate concepts∟ ∟ ∟ ∟ ∟ Fanconi Syndrome 34 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ Fanconi Syndrome ∟ ∟ ∟ ∟ ∟ Fanconi Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Fanconi Syndrome ∟ ∟ ∟ ∟ Fanconi Syndrome ∟ ∟ ∟ ∟ ∟ Fanconi Syndrome ∟ ∟ ∟ ∟ ∟ Fanconi Syndrome |
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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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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activeMeSHYear*: | 2007X |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1965-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Fanconin oireyhtymä (fi) XFanconin syndrooma (fi, replaced) Fanconis syndrom (sv) Renal Fanconi Syndrome (en, replaced) Proximal Renal Tubular Dysfunction (en, replaced) Fanconi Renotubular Syndrome (en, replaced) Lignac-Fanconi Syndrome (en, replaced) De Toni-Debre-Fanconi Syndrome (en, replaced) Syndroma Fanconi (la-FI, replaced) |
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