long chain acyl-CoA dehydrogenase deficiency
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Summary
long chain acyl-CoA dehydrogenase deficiency is a class of disease[1].
Key Facts
- long chain acyl-CoA dehydrogenase deficiency's instance of is recorded as class of disease[2].
- long chain acyl-CoA dehydrogenase deficiency's subclass of is recorded as metabolic disease due to other fatty acid oxidation disorder[3].
- long chain acyl-CoA dehydrogenase deficiency's subclass of is recorded as fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy[4].
- long chain acyl-CoA dehydrogenase deficiency's subclass of is recorded as acyl-CoA dehydrogenase deficiency[5].
- long chain acyl-CoA dehydrogenase deficiency's MeSH descriptor ID is recorded as C535690[6].
- long chain acyl-CoA dehydrogenase deficiency's Orphanet ID is recorded as 99900[7].
- long chain acyl-CoA dehydrogenase deficiency's NCI Thesaurus ID is recorded as C84537[8].
- long chain acyl-CoA dehydrogenase deficiency's genetic association is recorded as ACADL[9].
- long chain acyl-CoA dehydrogenase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99900[10].
- long chain acyl-CoA dehydrogenase deficiency's UMLS CUI is recorded as C0220711[11].
- long chain acyl-CoA dehydrogenase deficiency's ICD-10-CM is recorded as E71.3[12].
- long chain acyl-CoA dehydrogenase deficiency's Mondo ID is recorded as MONDO_0020531[13].