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Details for phenotype: X-linked hypophosphatemic rickets

EndoNet ID: ENP00119

Name

X-linked hypophosphatemic rickets

General information

This phenotype is not pathologic

Links to other resources

GO
OMIM 307800
Medline Plus 000344
Disease database 6513

Phenotype triggers

  • VDR
    in bone
    • Elevated circulating FGF23 levels have been found in most, but not all, patients with XLH. [1]
Reference