Number of the records: 1
hemoglobinopatie
SYS d006453 LBL 00000nz--a2200000n--4500 005 20250606214220.3 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 065 $a C15.378.420 065 $a C16.320.365 066 $a 01 $c 03 150 $a hemoglobinopatie $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 choroby hemoglobínu $2 slo 550 $7 sllk_us_auth*d006455 $Y Hemoglobins, Abnormal $w p $a hemoglobíny abnormálne 550 $7 sllk_us_auth*d006455 $Y Hemoglobins, Abnormal $w b $a hemoglobíny abnormálne 665 $a 68 $2 eng 680 9-
$i A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. $2 eng 680 $a do not confuse with HEMOGLOBINS, ABNORMAL (D12): use term in the text; coord IM with specific abnormal hemoglobin (IM) but HEMOGLOBIN C DISEASE; THALASSEMIA (hemoglobin H disease) & ANEMIA, SICKLE CELL (hemoglobin S disease) are available $2 eng 750 -2
$a Hemoglobinopathies $2 eng 980 $x M
Number of the records: 1