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(Q17116)
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Revision as of 20:48, 29 December 2023 by
Fire
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Created claim:
exact match
(P409)
: http://www.orpha.net/ORDO/Orphanet_207)
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Statements
instance of
developmental defect during embryogenesis
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designated intractable/rare diseases
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rare disease
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class of disease
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symptom or sign
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subclass of
craniosynostosis
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craniostenosis associated with a strabismus
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syndromic craniosynostosis
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disease
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health specialty
medical genetics
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exact match
http://purl.obolibrary.org/obo/DOID_2339
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http://identifiers.org/doid/DOID:2339
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http://purl.obolibrary.org/obo/HP_0004439
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http://www.orpha.net/ORDO/Orphanet_207
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Sitelinks
⧼wikibase-sitelinks-mywikigroup⧽
(0 entries)
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