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Fanconi Anemia
Hierarchy: | ∟ ∟ ∟ ∟ Fanconi Anemia 11 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Fanconi Anemia 11 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Fanconi Anemia 11 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Fanconi Anemia 11 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | |
Annotation: | do not confuse with FANCONI SYNDROME, a dysfunction of proximal renal tubules
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historyNote*: | 2002(1975); was see under ANEMIA, APLASTIC 1975-1990
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publicMeSHNote*: | 2002; see FANCONI'S ANEMIA 1991-2001; was see under ANEMIA, APLASTIC 1975-1990
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Scope note: | Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, August 20, 2004)
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activeMeSHYear*: | |
dateCreated*: | 1974-11-11X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2005-06-30X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Fanconin anemia (fi) XFanconi's Anemia (en, replaced) Anemia, Fanconi (en, replaced) Anemia de Fanconi (es) αναιμία Fanconi (el) Fanconi-Anämie (de) Fanconiho anémie (cs) Anämie, Fanconi- (de, replaced) |
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