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Familial Hypophosphatemic Rickets  

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Tipo

  • mesh:Descriptor

Definición

  • A hereditary disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. Autosomal and X-linked dominant and recessive variants have been reported. An X-linked recessive disorder associated with mutations in CLCN5, CHLORIDE CHANNEL 5. An X-linked disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. This disorder is caused by mutations in PHEX PHOSPHATE REGULATING NEUTRAL ENDOPEPTIDASE.

Etiquetas alternativas

  • Generalized Resistance To 1,25-Dihydroxyvitamin D
  • Hereditary Hypophosphatemic Rickets
  • Hereditary Vitamin D-Resistant Rickets
  • Hypocalcemic Vitamin D-Resistant Rickets
  • Rickets, Hereditary Vitamin D-Resistant
  • Vitamin D-Resistant Rickets, Hereditary
  • Vitamin D-Resistant Rickets With End-Organ Unresponsiveness To 1,25-Dihydroxycholecalciferol

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-LS30JRWF-J

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