Number of the records: 1
polyendokrinopatie autoimunitné
SYS d016884 LBL 00000cz--a2200000n--4500 005 20250606213905.0 008 920502|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 $d BA006 $d BA006 065 $a C19.787 065 $a C20.111.750 066 $a 01 $c 03 150 $a polyendokrinopatie autoimunitné $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 450 $w v $a Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy $2 eng 450 $w v $a Autoimmune Syndrome Type II, Polyglandular $2 eng 450 $w v $a Autoimmune Syndrome Type I, Polyglandular $2 eng 450 $w v $a Polyglandular Type I Autoimmune Syndrome $2 eng 450 $w v $a Polyglandular Type II Autoimmune Syndrome $2 eng 450 $w v $a Schmidt's Syndrome $2 eng 450 $w v $a polyendokrinopatia-kandidiáza-ektodermálna dystrofia, autoimunitná $2 slo 450 $w v $a polyendokrinopatia-kandidóza-ektodermová dystrofia, autoimunitná $2 slo 450 $w v $a syndróm autoimunitný polyendokrinný, typ 2 $2 slo 450 $w v $a syndróm autoimunitnej polyendokrinopatie, typ 1 $2 slo 450 $w v $a syndróm polyglandulárny autoimunitný, typ I $2 slo 450 $w v $a syndróm polyglandulárny autoimunitný typu I $2 slo 450 $w v $a syndróm polyglandulárny autoimunitný, typ II $2 slo 450 $w v $a syndróm polyglandulárny autoimunitný typu II $2 slo 450 $w v $a diabetes mellitus, Addisonova choroba, myxedém $2 slo 450 $w v $a syndróm viacpočetnej endokrinnej deficiencie, typ 2 $2 slo 450 $w v $a syndróm polyglandulárnej deficiencie, typ 2 $2 slo 450 $w v $a Schmidtov syndróm $2 slo 665 $a 1992 $2 eng 665 $a Autoimmune Diseases (1968-1991) $2 eng 665 $a Endocrine Diseases (1978-1991) $2 eng 680 9-
$i Autoimmune diseases affecting multiple endocrine organs. Type I is characterized by childhood onset and chronic mucocutaneous candidiasis (CANDIDIASIS, CHRONIC MUCOCUTANEOUS), while type II exhibits any combination of adrenal insufficiency (ADDISON'S DISEASE), lymphocytic thyroiditis (THYROIDITIS, AUTOIMMUNE;), HYPOPARATHYROIDISM; and gonadal failure. In both types organ-specific ANTIBODIES against a variety of ENDOCRINE GLANDS have been detected. The type II syndrome differs from type I in that it is associated with HLA-A1 and B8 haplotypes, onset is usually in adulthood, and candidiasis is not present. $2 eng 680 $a do not coordinate with specific endocrine disease term or CANDIDIASIS unless particularly discussed $2 eng 750 -2
$a Polyendocrinopathies, Autoimmune $2 eng 980 $x M
Number of the records: 1