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Item:Q16238: Difference between revisions
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Revision as of 20:30, 21 December 2023
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Created claim:
subclass of
(P1)
:
congenital disorder
(Q13932)
← Older edit
Latest revision as of 20:35, 21 December 2023
Fire
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talk
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contribs
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Bureaucrats
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Created claim:
exact match
(P409)
: http://www.orpha.net/ORDO/Orphanet_2140
(10 intermediate revisions by the same user not shown)
Property /
subclass of
rare genetic developmental defect during embryogenesis
Property /
subclass of
:
rare genetic developmental defect during embryogenesis
/ rank
Normal rank
Property /
subclass of
rare genetic respiratory disease
Property /
subclass of
:
rare genetic respiratory disease
/ rank
Normal rank
Property /
subclass of
disease
Property /
subclass of
:
disease
/ rank
Normal rank
Property /
has effect
asphyxia neonatorum
Property /
has effect
:
asphyxia neonatorum
/ rank
Normal rank
Property /
afflicts
thoracic diaphragm
Property /
afflicts
:
thoracic diaphragm
/ rank
Normal rank
Property /
health specialty
medical genetics
Property /
health specialty
:
medical genetics
/ rank
Normal rank
Property /
health specialty
pediatrics
Property /
health specialty
:
pediatrics
/ rank
Normal rank
Property /
exact match
http://purl.obolibrary.org/obo/DOID_3827
Property /
exact match
:
http://purl.obolibrary.org/obo/DOID_3827
/ rank
Normal rank
Property /
exact match
http://identifiers.org/doid/DOID:3827
Property /
exact match
:
http://identifiers.org/doid/DOID:3827
/ rank
Normal rank
Property /
exact match
http://purl.obolibrary.org/obo/HP_0000776
Property /
exact match
:
http://purl.obolibrary.org/obo/HP_0000776
/ rank
Normal rank
Property /
exact match
http://www.orpha.net/ORDO/Orphanet_2140
Property /
exact match
:
http://www.orpha.net/ORDO/Orphanet_2140
/ rank
Normal rank