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hypofosfatémia familiárna
SYS d007015 LBL 00000cz--a2200000o--4500 005 20250606213834.6 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C12.050.351.968.419.815.647 065 $a C12.200.777.419.815.647 065 $a C12.950.419.815.647 065 $a C16.320.565.618.544 065 $a C16.320.831.647 065 $a C18.452.648.618.544 065 $a C18.452.750.400.500 066 $a 01 $c 03 150 $a hypofosfatémia familiárna $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 665 $a 1965 $2 eng 680 9-
$i An 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. $2 eng 680 $a a clinical entity: not for decreased blood phosphate levels ( = PHOSPHATES /blood) $2 eng 750 -2
$a Hypophosphatemia, Familial $2 eng 980 $x M
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