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Item:Q17142: Difference between revisions
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Revision as of 21:09, 29 December 2023
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Created claim:
subclass of
(P1)
:
congenital disorder
(Q13932)
← Older edit
Latest revision as of 21:19, 29 December 2023
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Created claim:
exact match
(P409)
: http://www.orpha.net/ORDO/Orphanet_3388
(7 intermediate revisions by the same user not shown)
Property /
subclass of
congenital vertebral anomaly
Property /
subclass of
:
congenital vertebral anomaly
/ rank
Normal rank
Property /
subclass of
rare genetic developmental defect during embryogenesis
Property /
subclass of
:
rare genetic developmental defect during embryogenesis
/ rank
Normal rank
Property /
subclass of
genetic nervous system disorder
Property /
subclass of
:
genetic nervous system disorder
/ 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_0080074
Property /
exact match
:
http://purl.obolibrary.org/obo/DOID_0080074
/ rank
Normal rank
Property /
exact match
http://identifiers.org/doid/DOID:0080074
Property /
exact match
:
http://identifiers.org/doid/DOID:0080074
/ rank
Normal rank
Property /
exact match
http://purl.obolibrary.org/obo/HP_0002144
Property /
exact match
:
http://purl.obolibrary.org/obo/HP_0002144
/ rank
Normal rank
Property /
exact match
http://www.orpha.net/ORDO/Orphanet_3388
Property /
exact match
:
http://www.orpha.net/ORDO/Orphanet_3388
/ rank
Normal rank