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Nephritis, Hereditary
Hierarchy: | ∟ ∟ ∟ ∟ Nephritis, Hereditary 17 coordinate concepts∟ ∟ ∟ ∟ Nephritis, Hereditary 17 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Nephritis, Hereditary 17 coordinate concepts∟ ∟ ∟ Nephritis, Hereditary 17 coordinate concepts∟ ∟ ∟ ∟ ∟ Nephritis, Hereditary 17 coordinate concepts∟ ∟ ∟ ∟ Nephritis, Hereditary 17 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ Nephritis, Hereditary ∟ ∟ ∟ ∟ Nephritis, Hereditary ∟ ∟ ∟ ∟ ∟ ∟ Nephritis, Hereditary ∟ ∟ ∟ Nephritis, Hereditary ∟ ∟ ∟ ∟ ∟ Nephritis, Hereditary ∟ ∟ ∟ ∟ Nephritis, Hereditary |
historyNote*: | 77; was ALPORT'S SYNDROME 1964-76 (Prov 1964-69)
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onlineNote*: | use NEPHRITIS, HEREDITARY to search ALPORT'S SYNDROME 1966-76 (as Prov 1966-69)
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publicMeSHNote*: | 77; was ALPORT'S SYNDROME 1970-76
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Scope note: | A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE.
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activeMeSHYear*: | 2007X |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1970-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | NLMX |
Type: | |
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Labels and equivalent concepts: | Perinnöllinen munuaistulehdus (fi) XAlport's Syndrome (en, replaced) Nephritis, Familial (en, replaced) Nefritis Hereditaria (es) κληρονομική νεφρίτιδα (el) Nephritis, hereditäre (de) nefritida dědičná (cs) Nefritis Familiar (es, replaced) Síndrome de Alport (es, replaced) Nephropathie-Taubheits-Syndrom, hereditäres (de, replaced) Nephritis, familiäre (de, replaced) Alport-Syndrom, autosomal dominantes (de, replaced) Alport-Syndrom, autosomal rezessives (de, replaced) Alport-Syndrom, X-Chromosom-gebundenes (de, replaced) Alport-Syndrom (de, replaced) |
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