Concept information
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Urologic Diseases
Kidney Diseases
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
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Urologic Diseases
Kidney Diseases
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
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Genetic Diseases, Inborn
Metabolism, Inborn Errors
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
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Metabolic Diseases
Metabolism, Inborn Errors
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
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Genetic Diseases, Inborn
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Hypophosphatemia, Familial
Término preferido
Familial Hypophosphatemic Rickets
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Tipo
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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.
Concepto genérico
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
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francés
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Rachitisme hypophosphatémique héréditaire
URI
http://data.loterre.fr/ark:/67375/JVR-LS30JRWF-J
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