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hypofosfatémia familiárna

  1. Record numberd007015
    Date06.06.2025
    TypeM - MESH
    Topical termhypofosfatémia familiárna
    UDCC12.050.351.968.419.815.647C12.200.777.419.815.647C12.950.419.815.647C16.320.565.618.544C16.320.831.647C18.452.648.618.544C18.452.750.400.500
    NoteAn inherited condition of abnormally low serum levels of PHOSPHATES (below 1 mg/liter) which can occur in a number of genetic diseases with defective reabsorption of inorganic phosphorus by the PROXIMAL RENAL TUBULES. This leads to phosphaturia, HYPOPHOSPHATEMIA, and disturbances of cellular and organ functions such as those in X-LINKED HYPOPHOSPHATEMIC RICKETS; OSTEOMALACIA; and FANCONI SYNDROME.
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Number of the records: 1  

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