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Summary Literature (0)
MIM:145000 - HYPERPARATHYROIDISM 1; HRPT1

Xenbase Genes: men1, cdc73

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007767 - hyperparathyroidism 1
MONDO:0015027 - manual digit 3 phalanx endochondral element
MONDO:0020523 - familial parathyroid adenoma

Disease Ontology (DO):
DOID:13543 - hyperparathyroidism