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(Q22008)

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Statements

instance of
developmental defect during embryogenesis
0 references
class of disease
0 references
subclass of
rare parathyroid disease and phosphocalcic metabolism anomaly
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primary bone dysplasia with defective bone mineralization
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rare genetic parathyroid disease and phosphocalcic metabolism disorder
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vitamin metabolic disorder
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exact match
http://www.orpha.net/ORDO/Orphanet_289098
0 references
 

Sitelinks

⧼wikibase-sitelinks-mywikigroup⧽(0 entries)

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    Retrieved from "https://wiki.tiffa.net/w/index.php?title=Item:Q22008&oldid=138078"
    Last edited on 12 April 2024, at 20:31

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