Počet záznamov: 1
hypertyroxinémia familiárna dysalbuminemická
SYS d050010 LBL 00000nx--j22000003--45-- 005 20240119200513.6 100 $a 20050630csloy0103----ba0 152 $b mesh 250 $a hypertyroxinémia familiárna dysalbuminemická $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 300 1-
$a 2006 $8 eng 300 1-
$a Serum Albumin (1982-2005) $8 eng 300 1-
$a Thyroxine (1982-2005) $8 eng 330 1-
$a An inherited autosomal dominant trait characterized by abnormally elevated levels of total serum THYROXINE; (T4) in euthyroid patients with abnormal SERUM ALBUMIN that binds T4 with enhanced affinity. The serum levels of free T4, free T3, and TSH are normal. It is one of several T4 abnormalities produced by non-thyroid disorder. This condition is due to mutations of the ALB gene on CHROMOSOME 4. $8 eng 686 $a C16.320.427 686 $a C19.874.410.249 750 $a Hyperthyroxinemia, Familial Dysalbuminemic $8 eng 801 -0
$a US $b DNLM $c 20050630 801 -2
$a SK $b BA006 $c 20060227 980 $x M
Počet záznamov: 1