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About:
Lipoyl transferase 2 deficiency
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An Entity of Type :
wikibase:Item
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associated with source
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Type:
Item
New Facet based on Instances of this Class
human disease
Attributes
Values
rdf:type
Item
description
human disease
(en)
хвороба людини
(uk)
exact match
wds:Q55788240-D5DCEE81-B5F1-41E0-AFF8-C438A6F71EB6
exact match
http://www.orpha.net/ORDO/Orphanet_447795
Mondo ID
wds:Q55788240-AAC041C8-392F-49D2-A022-3DEE0BA9541E
Mondo ID
http://purl.obolibrary.org/obo/MONDO_0018651
Mondo ID
MONDO_0018651
rdfs:label
Lipoyl transferase 2 deficiency
(en)
skos:prefLabel
Lipoyl transferase 2 deficiency
(en)
name
Lipoyl transferase 2 deficiency
(en)
instance of
wds:Q55788240-5A626BAC-CEBE-4B0D-A5F7-0BF79DDC93BA
instance of
class of disease
subclass of
wds:Q55788240-531FC827-5C11-4E0F-ADBB-6D3629099F35
subclass of
biological anomaly without phenotypic characterization
Orphanet ID
wds:Q55788240-9CE80737-4AC1-4D10-854A-7998B74A4672
Orphanet ID
447795
UMLS CUI
wds:Q55788240-0B7FCA2A-7E87-4608-8397-03EB033F2048
UMLS CUI
C5681203
is
about
of
https://www.wikidata.org/wiki/Special:EntityData/Q55788240
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