Počet záznamov: 1
pseudohypoparatyreóza
SYS d011547 LBL 00000cz--a2200000n--4500 005 20250606213326.5 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 065 $a C05.116.198.709 065 $a C16.320.565.618.815 065 $a C18.452.104.709 065 $a C18.452.174.766 065 $a C18.452.648.618.815 066 $a 01 $c 03 150 $a pseudohypoparatyreóza $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 Albright Hereditary Osteodystrophy $2 eng 450 $w v $a PHPIa $2 eng 450 $w v $a Albrightova dedičná osteodystrofia $2 slo 450 $w v $a Albrightova hereditárna osteodystrofia $2 slo 450 $w v $a Albrightova hereditárna osteodystrofia s mnohonásobnou hormonálnou rezistenciou $2 slo 450 $w v $a pseudohypoparatyreoidizmus $2 slo 450 $w v $a PHPIa $2 slo 450 $w v $a PHP Ia $2 slo 450 $w v $a PHD1b $2 slo 450 $w v $a PHD Ib $2 slo 550 $7 sllk_us_auth*d019205 $Y GTP-Binding Protein alpha Subunits, Gs $w p $a alfa podjednotky proteínu viažuceho GTP, Gs 550 $7 sllk_us_auth*d019205 $Y GTP-Binding Protein alpha Subunits, Gs $w b $a alfa podjednotky proteínu viažuceho GTP, Gs 665 $a 65(63) $2 eng 680 9-
$i A hereditary syndrome clinically similar to HYPOPARATHYROIDISM. It is characterized by HYPOCALCEMIA; HYPERPHOSPHATEMIA; and associated skeletal development impairment and caused by failure of response to PARATHYROID HORMONE rather than deficiencies. A severe form with resistance to multiple hormones is referred to as Type 1a and is associated with maternal mutant allele of the ALPHA CHAIN OF STIMULATORY G PROTEIN. $2 eng 680 $a do not confuse with PSEUDOPSEUDOHYPOPARATHYROIDISM $2 eng 750 -2
$a Pseudohypoparathyroidism $2 eng 980 $x M
Počet záznamov: 1