| Descriptor English: | Hypophosphatemia, Familial | ||||
| Descriptor Spanish: |
Hipofosfatemia Familiar
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| Descriptor Portuguese: | Hipofosfatemia Familiar | ||||
| Descriptor French: | Hypophosphatémie familiale | ||||
| Entry term(s): |
Diabetes, Phosphate Familial Hypophosphatemia Familial Hypophosphatemias Hyperphosphaturia Hypophosphatemias, Familial Phosphate Diabetes Phosphaturia |
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| Tree number(s): |
C12.050.351.968.419.815.647 C12.200.777.419.815.647 C12.950.419.815.647 C16.320.565.618.544 C16.320.831.647 C18.452.648.618.544 C18.452.750.400.500 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D007015 | ||||
| Scope note: | 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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| Annotation: | a clinical entity: not for decreased blood phosphate levels ( = PHOSPHATES /blood) |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 1965 |
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| History Note: | 1965 |
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| DeCS ID: | 7194 | ||||
| Unique ID: | D007015 | ||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
| Date Established: | 1965/01/01 | ||||
| Date of Entry: | 1999/01/01 | ||||
| Revision Date: | 2006/07/05 |
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Hypophosphatemia, Familial
- Preferred
Phosphaturia
- Related but not broader or narrower
| Concept UI |
M0010916 |
| Scope note | 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. |
| Preferred term | Hypophosphatemia, Familial |
| Entry term(s) |
Familial Hypophosphatemia Familial Hypophosphatemias Hypophosphatemias, Familial |
| Concept UI |
M0010918 |
| Preferred term | Phosphaturia |
| Entry term(s) |
Diabetes, Phosphate Hyperphosphaturia Phosphate Diabetes |
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