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Summary Literature (0)
MIM:193100 - HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT; ADHR

Xenbase Genes: fgf23.2, fgf23

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008660 - autosomal dominant hypophosphatemic rickets

Disease Ontology (DO):
DOID:0050948 - autosomal dominant hypophosphatemic rickets