SHMARQL
Docs
Query
Entity
Story editor
acyl-CoA dehydrogenase deficiency
<http:/
/
www.wikidata.org/
entity/
Q55787302>
human disease
rdfs:
label
en
fr
pt
pt-br
sl
"Déficit de acil-CoA desidrogenase"
@pt
"Déficit de acil-CoA desidrogenase"
@pt-br
"acyl-CoA dehydrogenase deficiency"
@en
"déficit en acyl-CoA déshydrogénase"
@fr
"pomanjkanje acil-CoA dehidrogenaze"
@sl
schema:
description
en
uk
"human disease"
@en
"хвороба людини"
@uk
schema:
date
Modified
"2026-10-24T00:02:33+00:00"
^^xsd:dateTime
schema:
version
2560161790
wikibase:
identifiers
5
wikibase:
sitelinks
0
wikibase:
statements
15
p:
P14914
wd:
statement/Q55787302-8B3580C9-A6D5-460A-842F-15EA3ACEDE1F
p:
P1550
wd:
statement/Q55787302-7BE08A15-3073-4436-B384-6CB19859D8FC
p:
P2293
wd:
statement/Q55787302-4106947E-6A06-4F9F-9BD9-F8A17060C008
wd:
statement/Q55787302-5EF5AFD9-CF9B-4425-B684-07030A427040
wd:
statement/Q55787302-90951D33-86F2-4A2B-AB36-0F11424C8572
wd:
statement/Q55787302-AD53C3BB-85BA-4FCB-B349-BD31C5367306
wd:
statement/Q55787302-C04672C3-7C74-4966-B183-94F5187621AA
wd:
statement/Q55787302-FC1254EB-1B10-4449-967C-A364E2996613
wd:
statement/Q55787302-FE421A48-4647-47B1-81EF-271B8304A5B5
p:
P279
wd:
statement/Q55787302-5422C291-06E5-419A-941D-9E13A5E5EB5C
p:
P2888
wd:
statement/Q55787302-6F841FF9-EFA2-46A4-80D2-245B87F0E96B
p:
P2892
wd:
statement/Q55787302-6CB6BCD7-0179-4DCE-BE4F-340A7125776F
p:
P31
wd:
statement/Q55787302-F006D8D5-2BFE-458C-82CB-675E67438825
p:
P4229
wd:
statement/Q55787302-DB315ABE-188A-4723-A8B1-FB06344D472F
p:
P5270
wd:
statement/Q55787302-E35C9D2F-092C-42E8-A7F5-49DB1F55F4A1
p:
direct-
normalized/
P5270
<http:/
/
purl.obolibrary.org/
obo/
MONDO_0017714>
wdt:
P14914
"D309120"
wdt:
P1550
"309120"
wdt:
P2293
ETFDH
ETFA
ETFB
FLAD1
SLC25A32
ACADS
ACADM
wdt:
P279
disorder of fatty acid oxidation and ketogenesis
wdt:
P2888
<http:/
/
www.orpha.net/
ORDO/
Orphanet_309120>
wdt:
P2892
"C0268635"
wdt:
P31
type of disease
wdt:
P4229
"E71.3"
wdt:
P5270
"MONDO_0017714"
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data from SPARQL profile:
Wikidata