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Summary Literature (0)
MIM:610071 - HYPERPARATHYROIDISM 3; HRPT3

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012406 - hyperparathyroidism 3
MONDO:0015027 - manual digit 3 phalanx endochondral element

Disease Ontology (DO):
DOID:13543 - hyperparathyroidism