C1704981_NCI_NICHD | Knowledge4COVID-19

Property	Value
?:definition	An autosomal dominant condition that may be associated with mutation(s) in the CDC73 gene, encoding cell division cycle protein 73 homolog. The condition is characterized by hyperfunctioning parathyroid adenomas and fibro-osseous tumors of the maxilla and mandible. This condition may also be associated with parathyroid carcinoma, Wilms tumor, and Hurthle cell thyroid adenomas.
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?:type	<https://research.tib.eu/covid-19/vocab/AnnotationDefinition>

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