multiple acyl-CoA dehydrogenase deficiency
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multiple acyl-CoA dehydrogenase deficiency
Summary
multiple acyl-CoA dehydrogenase deficiency is a designated intractable/rare disease[1]. It draws 20 Wikipedia views per month (designated_intractable_rare_disease category, ranking #153 of 201).[2]
Key Facts
- multiple acyl-CoA dehydrogenase deficiency's image is recorded as Glutaric-acid-3D-balls.png[3].
- multiple acyl-CoA dehydrogenase deficiency's instance of is recorded as designated intractable/rare disease[4].
- multiple acyl-CoA dehydrogenase deficiency's instance of is recorded as class of disease[5].
- multiple acyl-CoA dehydrogenase deficiency's subclass of is recorded as inherited metabolic disorder[6].
- multiple acyl-CoA dehydrogenase deficiency's subclass of is recorded as acyl-CoA dehydrogenase deficiency[7].
- multiple acyl-CoA dehydrogenase deficiency's subclass of is recorded as fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy[8].
- multiple acyl-CoA dehydrogenase deficiency's subclass of is recorded as genetic disease[9].
- multiple acyl-CoA dehydrogenase deficiency's subclass of is recorded as glutaric aciduria[10].
- multiple acyl-CoA dehydrogenase deficiency's MeSH descriptor ID is recorded as D054069[11].
- multiple acyl-CoA dehydrogenase deficiency's OMIM ID is recorded as 231680[12].
- multiple acyl-CoA dehydrogenase deficiency's ICD-9 ID is recorded as 277.85[13].
- multiple acyl-CoA dehydrogenase deficiency's DiseasesDB is recorded as 29816[14].
- multiple acyl-CoA dehydrogenase deficiency's GeneReviews ID is recorded as NBK558236[15].
- multiple acyl-CoA dehydrogenase deficiency's MeSH tree code is recorded as C16.320.565.100.614[16].
- multiple acyl-CoA dehydrogenase deficiency's MeSH tree code is recorded as C18.452.648.100.614[17].
- multiple acyl-CoA dehydrogenase deficiency's MeSH tree code is recorded as C18.452.660.612[18].
- multiple acyl-CoA dehydrogenase deficiency's Disease Ontology ID is recorded as DOID:0060358[19].
- multiple acyl-CoA dehydrogenase deficiency's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4819[20].
- multiple acyl-CoA dehydrogenase deficiency's Orphanet ID is recorded as 26791[21].
- multiple acyl-CoA dehydrogenase deficiency's NCI Thesaurus ID is recorded as C99102[22].
- multiple acyl-CoA dehydrogenase deficiency's NCI Thesaurus ID is recorded as C84907[23].
- multiple acyl-CoA dehydrogenase deficiency's health specialty is recorded as medical genetics[24].
- multiple acyl-CoA dehydrogenase deficiency's health specialty is recorded as endocrinology[25].
- multiple acyl-CoA dehydrogenase deficiency's genetic association is recorded as ETFB[26].
- multiple acyl-CoA dehydrogenase deficiency's genetic association is recorded as ETFA[27].
Why It Matters
multiple acyl-CoA dehydrogenase deficiency draws 20 Wikipedia views per month (designated_intractable_rare_disease category, ranking #153 of 201).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] It is known by 24 alternative names across languages and contexts.[29]