syndrome de Laron (Q669822)

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congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration anglais
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syndrome de Laron
Aucune description fournie
    anglais
    Laron syndrome
    congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration
    • Laron-type isolated somatotropin defect (disorder)
    • Laron-type isolated somatotropin defect
    • Growth Hormone Receptor Deficiency
    • Primary growth hormone resistance
    • Laron-type dwarfism
    • Pituitary Dwarfism 2
    • Growth Hormone Insensitivity Syndrome
    • Primary GH insensitivity
    • Short stature due to growth hormone resistance
    • Complete growth hormone insensitivity
    • Primary GH resistance
    • GH receptor deficiency
    • Primary growth hormone insensitivity

    Déclarations

    Identifiants

    arborescence MeSH
    C05.116.099.343.679
    0 référence
    C16.320.240.750
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    C19.297.656
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    identifiant KEGG
    H02037
    0 référence
    UniProt disease ID anglais
    DI-01877
    0 référence
     
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                    Récupérée de « https://www.wikidata.org/w/index.php?title=Q669822&oldid=2180132553 »