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Item:Q17588: Difference between revisions
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Revision as of 11:26, 31 December 2023
Fire
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talk
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Bureaucrats
,
Interface administrators
,
Administrators
132,738
edits
Created claim:
instance of
(P2)
:
class of disease
(Q5294)
← Older edit
Latest revision as of 21:02, 31 December 2023
Fire
(
talk
|
contribs
)
Bureaucrats
,
Interface administrators
,
Administrators
132,738
edits
Created claim:
exact match
(P409)
: http://www.orpha.net/ORDO/Orphanet_905
(27 intermediate revisions by the same user not shown)
Property /
instance of
symptom or sign
Property /
instance of
:
symptom or sign
/ rank
Normal rank
Property /
subclass of
liver disease
Property /
subclass of
:
liver disease
/ rank
Normal rank
Property /
subclass of
metal metabolism disorder
Property /
subclass of
:
metal metabolism disorder
/ rank
Normal rank
Property /
subclass of
copper metabolism disease
Property /
subclass of
:
copper metabolism disease
/ rank
Normal rank
Property /
subclass of
organic brain syndrome
Property /
subclass of
:
organic brain syndrome
/ rank
Normal rank
Property /
subclass of
rare hereditary metabolic disease with peripheral neuropathy
Property /
subclass of
:
rare hereditary metabolic disease with peripheral neuropathy
/ rank
Normal rank
Property /
subclass of
metabolic disease with cataract
Property /
subclass of
:
metabolic disease with cataract
/ rank
Normal rank
Property /
subclass of
metabolic disease with corneal opacity
Property /
subclass of
:
metabolic disease with corneal opacity
/ rank
Normal rank
Property /
subclass of
supranuclear oculomotor palsy
Property /
subclass of
:
supranuclear oculomotor palsy
/ rank
Normal rank
Property /
subclass of
tremor
Property /
subclass of
:
tremor
/ rank
Normal rank
Property /
subclass of
rare genetic tremor disorder
Property /
subclass of
:
rare genetic tremor disorder
/ rank
Normal rank
Property /
subclass of
rare metabolic liver disease
Property /
subclass of
:
rare metabolic liver disease
/ rank
Normal rank
Property /
subclass of
metal transport or utilization disorder with epilepsy
Property /
subclass of
:
metal transport or utilization disorder with epilepsy
/ rank
Normal rank
Property /
subclass of
rare genetic epilepsy
Property /
subclass of
:
rare genetic epilepsy
/ rank
Normal rank
Property /
subclass of
neurometabolic disease
Property /
subclass of
:
neurometabolic disease
/ rank
Normal rank
Property /
subclass of
rare disorder with dystonia and other neurologic or systemic manifestation
Property /
subclass of
:
rare disorder with dystonia and other neurologic or systemic manifestation
/ rank
Normal rank
Property /
subclass of
nephropathy secondary to a storage or other metabolic disease
Property /
subclass of
:
nephropathy secondary to a storage or other metabolic disease
/ rank
Normal rank
Property /
subclass of
disease
Property /
subclass of
:
disease
/ rank
Normal rank
Property /
has cause
genetics
Property /
has cause
:
genetics
/ rank
Normal rank
Property /
health specialty
endocrinology
Property /
health specialty
:
endocrinology
/ rank
Normal rank
Property /
symptoms and signs
edema
Property /
symptoms and signs
:
edema
/ rank
Normal rank
Property /
symptoms and signs
jaundice
Property /
symptoms and signs
:
jaundice
/ rank
Normal rank
Property /
symptoms and signs
personality changes
Property /
symptoms and signs
:
personality changes
/ rank
Normal rank
Property /
symptoms and signs
blue nails
Property /
symptoms and signs
:
blue nails
/ rank
Normal rank
Property /
symptoms and signs
face of the giant panda sign
Property /
symptoms and signs
:
face of the giant panda sign
/ rank
Normal rank
Property /
exact match
http://purl.obolibrary.org/obo/DOID_893
Property /
exact match
:
http://purl.obolibrary.org/obo/DOID_893
/ rank
Normal rank
Property /
exact match
http://identifiers.org/doid/DOID:893
Property /
exact match
:
http://identifiers.org/doid/DOID:893
/ rank
Normal rank
Property /
exact match
http://www.orpha.net/ORDO/Orphanet_905
Property /
exact match
:
http://www.orpha.net/ORDO/Orphanet_905
/ rank
Normal rank