Počet záznamov: 1
amyloidóza
SYS d000686 LBL 00000cx--j2200000---45-- 005 20240119201511.6 100 $a 19990101asloy0103----ba0 152 $b mesh 250 $a amyloidóza $x BL $x CF $x CI $x CL $x CN $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 $8 slo 330 1-
$a A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits. $8 eng 550 $3 sllk_un_auth*d000682 $Y Amyloid $5 B $a amyloid 550 $3 sllk_un_auth*d000682 $Y Amyloid $5 F $a amyloid 550 $3 sllk_un_auth*d008232 $Y Lymphoproliferative Disorders $5 F $a poruchy lymfoproliferatívne 550 $3 sllk_un_auth*d010265 $Y Paraproteinemias $5 F $a paraproteinémie 550 $3 sllk_un_auth*d058225 $Y Plaque, Amyloid $5 B $a plak amyloidný 686 $a C18.452.845.500 750 $a Amyloidosis $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20070706 820 $a coord IM with organ/dis precoord (IM); /genet: consider also AMYLOIDOSIS, HEREDITARY $8 eng 980 $x M
Počet záznamov: 1