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Item:Q17116: Difference between revisions
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Revision as of 20:24, 29 December 2023
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Created claim:
instance of
(P2)
:
developmental defect during embryogenesis
(Q13937)
← Older edit
Latest revision as of 20:48, 29 December 2023
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talk
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Bureaucrats
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Created claim:
exact match
(P409)
: http://www.orpha.net/ORDO/Orphanet_207
(12 intermediate revisions by the same user not shown)
Property /
instance of
designated intractable/rare diseases
Property /
instance of
:
designated intractable/rare diseases
/ rank
Normal rank
Property /
instance of
rare disease
Property /
instance of
:
rare disease
/ rank
Normal rank
Property /
instance of
class of disease
Property /
instance of
:
class of disease
/ rank
Normal rank
Property /
instance of
symptom or sign
Property /
instance of
:
symptom or sign
/ rank
Normal rank
Property /
subclass of
craniosynostosis
Property /
subclass of
:
craniosynostosis
/ rank
Normal rank
Property /
subclass of
craniostenosis associated with a strabismus
Property /
subclass of
:
craniostenosis associated with a strabismus
/ rank
Normal rank
Property /
subclass of
syndromic craniosynostosis
Property /
subclass of
:
syndromic craniosynostosis
/ rank
Normal rank
Property /
subclass of
disease
Property /
subclass of
:
disease
/ rank
Normal rank
Property /
health specialty
medical genetics
Property /
health specialty
:
medical genetics
/ rank
Normal rank
Property /
exact match
http://purl.obolibrary.org/obo/DOID_2339
Property /
exact match
:
http://purl.obolibrary.org/obo/DOID_2339
/ rank
Normal rank
Property /
exact match
http://identifiers.org/doid/DOID:2339
Property /
exact match
:
http://identifiers.org/doid/DOID:2339
/ rank
Normal rank
Property /
exact match
http://purl.obolibrary.org/obo/HP_0004439
Property /
exact match
:
http://purl.obolibrary.org/obo/HP_0004439
/ rank
Normal rank
Property /
exact match
http://www.orpha.net/ORDO/Orphanet_207
Property /
exact match
:
http://www.orpha.net/ORDO/Orphanet_207
/ rank
Normal rank