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Summary Literature (1)
MIM:307800 - HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR

Xenbase Genes: phex

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010619 - X-linked dominant hypophosphatemic rickets

Disease Ontology (DO):
DOID:0050445 - X-linked dominant hypophosphatemic rickets