Number of the records: 1
amyloidóza
SYS d000686 LBL 00000cz--a2200000n--4500 005 20250606213101.3 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C18.452.845.500 066 $a 01 $c 03 150 $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 $2 slo 550 $7 sllk_us_auth*d000682 $Y Amyloid $w b $a amyloid 550 $7 sllk_us_auth*d000682 $Y Amyloid $w p $a amyloid 550 $7 sllk_us_auth*d008232 $Y Lymphoproliferative Disorders $w p $a poruchy lymfoproliferatívne 550 $7 sllk_us_auth*d010265 $Y Paraproteinemias $w p $a paraproteinémie 550 $7 sllk_us_auth*d058225 $Y Plaque, Amyloid $w b $a plak amyloidný 680 9-
$i 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. $2 eng 680 $a coord IM with organ/dis precoord (IM); /genet: consider also AMYLOIDOSIS, HEREDITARY $2 eng 750 -2
$a Amyloidosis $2 eng 980 $x M
Number of the records: 1