multiple acyl-CoA dehydrogenase deficiency

medical condition
rdfs:label
"multiple acyl-CoA dehydrogenase deficiency"@en
skos:altLabel
"Etfa Deficiency"@en
"Etfb Deficiency"@en
"Etfdh Deficiency"@en
"Ethylmalonic-Adipicaciduria"@en
"Ga 2"@en
"Glutaric Acidemia 2"@en
"Glutaric Acidemia 2A"@en
"Glutaric Acidemia 2B"@en
"Glutaric Acidemia 2C"@en
"Glutaric Aciduria 2"@en
"Glutaric Aciduria, Type 2"@en
"Glutaric acidaemia type 2"@en
"MAD deficiency"@en
"MADD"@en
"MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY"@en
"MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY; MADD"@en
"Multiple Acyl Coenzyme A Dehydrogenase Deficiency"@en
"electron transfer flavoprotein deficiency"@en
"electron transfer flavoprotein ubiquinone oxidoreductase deficiency"@en
"glutaric acidemia type 2"@en
"glutaric aciduria type 2"@en
schema:description
"medical condition"@en
schema:dateModified "2026-10-23T23:52:35+00:00"^^xsd:dateTime
schema:version 2560159868
wikibase:identifiers 25
28
wikibase:sitelinks 5
wikibase:statements 51
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p:direct-normalized/P6366 <https://makg.org/entity/2776200808>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C16.320.565.100.614>
<http://id.nlm.nih.gov/mesh/C18.452.648.100.614>
<http://id.nlm.nih.gov/mesh/C18.452.660.612>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0060358>
wdt:P11143 "Glutaric acidemia type 2"
wdt:P1193 0.000005^^xsd:decimal
wdt:P1325 <http://www.nanbyou.or.jp/entry/4819>
wdt:P14914 "D26791"
wdt:P1550 "26791"
wdt:P1748 "C84907"
"C99102"
wdt:P18 <http://commons.wikimedia.org/wiki/Special:FilePath/Glutaric-acid-3D-balls.png>
wdt:P1995 medical genetics
endocrinology
wdt:P2293 ETFDH
ETFA
ETFB
FLAD1
SLC25A32
wdt:P279 glutaric aciduria
fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy
acyl-CoA dehydrogenase deficiency
wdt:P2841 any age
wdt:P2888 <http://identifiers.org/doid/DOID:0060358>
<http://purl.obolibrary.org/obo/DOID_0060358>
<http://www.orpha.net/ORDO/Orphanet_26791>
wdt:P2892 "C0268596"
"C1856401"
"C1856403"
"C1856405"
"C2931346"
"C3278154"
"C3278155"
"C3278156"
wdt:P31 type of disease
designated intractable/rare disease
wdt:P4229 "E71.3"
"E71.313"
wdt:P4233 "glutaric-acidemia-type-ii"
wdt:P4317 "6523"
wdt:P486 "D054069"
wdt:P492 "231680"
wdt:P493 "277.85"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0009282"
wdt:P557 "29816"
wdt:P6366 "2776200808"
wdt:P6532 skeletal muscle atrophy
wdt:P668 "NBK558236"
wdt:P672 "C16.320.565.100.614"
"C18.452.648.100.614"
"C18.452.660.612"
wdt:P699 "DOID:0060358"
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