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pseudohypoparatyreóza

  1. Record numberd011547
    Date06.06.2025
    TypeM
    Topical termpseudohypoparatyreóza
    Other termEnglish (Pseudonym) Albright Hereditary Osteodystrophy
    English (Pseudonym) PHPIa
    Slovak (Pseudonym) Albrightova dedičná osteodystrofia
    Slovak (Pseudonym) Albrightova hereditárna osteodystrofia
    Slovak (Pseudonym) Albrightova hereditárna osteodystrofia s mnohonásobnou hormonálnou rezistenciou
    Slovak (Pseudonym) pseudohypoparatyreoidizmus
    Slovak (Pseudonym) PHPIa
    Slovak (Pseudonym) PHP Ia
    Slovak (Pseudonym) PHD1b
    Slovak (Pseudonym) PHD Ib
    See also(Skutočné meno) alfa podjednotky proteínu viažuceho GTP, Gs
    (Later heading) alfa podjednotky proteínu viažuceho GTP, Gs
    UDCC05.116.198.709C16.320.565.618.815C18.452.104.709C18.452.174.766C18.452.648.618.815
    NoteA 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.
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