Počet záznamov: 1
Fanconiho anémia
SYS d005199 LBL 00000cz--a2200000n--4500 005 20250606214757.7 008 921111|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 065 $a C15.378.050.085.080.280 065 $a C15.378.190.223.500.500.280 065 $a C16.320.077.280 065 $a C18.452.284.280 066 $a 01 $c 03 150 $a Fanconiho anémia $x BL $x CF $x CI $x CL $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $2 slo 450 $w v $a Anemia, Fanconi $2 eng 450 $w v $a Fanconiho málokrvnosť $2 slo 450 $w v $a Fanconiho hypoplastická anémia $2 slo 450 $w v $a Fanconiho pancytopénia $2 slo 450 $w v $a Fanconiho panmyelopatia $2 slo 665 $a 2002(1975); was see under ANEMIA, APLASTIC 1975-1990 $2 eng 680 9-
$i 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) $2 eng 680 $a do not confuse with FANCONI SYNDROME, a dysfunction of proximal renal tubules $2 eng 750 -2
$a Fanconi Anemia $2 eng 980 $x M
Počet záznamov: 1