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familiární hypoadrenokorticismus

  1. Topical termfamiliární hypoadrenokorticismus
    See linkAddison Disease, X-Linked (UF)
    Adrenal Hypoplasia, Congenital (UF)
    Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism (UF)
    AHC with Isolated Gonadotropin Deficiency (UF)
    Complex Glycerol Kinase Deficiency (UF)
    Cytomegalic Adrenocortical Hypoplasia (UF)
    Familial X-linked Addison Disease (UF)
    X-linked Adrenal Hypoplasia (UF)
    X-linked Congenital Adrenal Hypoplasia (UF)
    Xp21 Contiguous Gene Deletion Syndrome (UF)
    See alsoAddisonova nemoc
    Linking entryHypoadrenocorticism, Familial
    ConspectC19. - 053. - 500. - 263. - 500
    NoteHereditary forms of Addison disease that may exhibit autosomal recessive or X-linked inheritance. They are characterized by severe neurological symptoms, APNEA; and death in infancy. OMIM: 240200
    DatabaseMESH
    References (1) - MESH
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Number of the records: 1  

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