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hypofosfatémia familiárna

Č. záznamu	d007015
Dátum	06.06.2025
Typ	M - MESH
Tematický termín	hypofosfatémia familiárna
MDT	C12.050.351.968.419.815.647C12.200.777.419.815.647C12.950.419.815.647C16.320.565.618.544C16.320.831.647C18.452.648.618.544C18.452.750.400.500
Poznámka	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.

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