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(Q17116)
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Revision as of 20:38, 29 December 2023 by
Fire
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Created claim:
subclass of
(P1)
:
craniosynostosis
(Q17117)
)
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Statements
instance of
developmental defect during embryogenesis
0 references
designated intractable/rare diseases
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rare disease
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class of disease
0 references
symptom or sign
0 references
subclass of
craniosynostosis
0 references
Sitelinks
⧼wikibase-sitelinks-mywikigroup⧽
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