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(Q22008)
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Revision as of 20:31, 12 April 2024 by
Fire
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Created claim:
exact match
(P409)
: http://www.orpha.net/ORDO/Orphanet_289098)
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Statements
instance of
developmental defect during embryogenesis
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class of disease
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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⧽
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