Visningssätt för begreppens/termernas förhållanden:
Det sätt begreppsrelationer visas:
Det sätt begreppsrelationer visas:
Fanconis anemi
Hierarki: | ∟ ∟ ∟ ∟ ∟ ∟ Fanconis anemi 11 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Fanconis anemi 11 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Fanconis anemi 11 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Fanconis anemi 11 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Bredare villkor: | |
Anmärkning: | 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)
X |
Annotation: | do not confuse with FANCONI SYNDROME, a dysfunction of proximal renal tubules
X |
historyNote*: | 2002(1975); was see under ANEMIA, APLASTIC 1975-1990
X |
publicMeSHNote*: | 2002; see FANCONI'S ANEMIA 1991-2001; was see under ANEMIA, APLASTIC 1975-1990
X |
activeMeSHYear*: | |
dateCreated*: | 1974-11-11X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2005-06-30X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | NLMX |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Fanconin anemia (fi) XAnemia, Fanconin (fi, ersatt) Fanconianemi (sv, ersatt) Fanconi Anemia (en) Fanconi's Anemia (en, ersatt) Anemia, Fanconi (en, ersatt) Anaemia Fanconi (la-FI, ersatt) |
Dela: |
Laddar resultat...