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Summary Literature (0)
MIM:617993 - TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2; HFTC2

Xenbase Genes: fgf23.2, fgf23

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0060714 - tumoral calcinosis, hyperphosphatemic, familial, 2