has material basis in germline mutation in disease has basis in disruption of disease caused by disruption of ACADVL very-long-chain fatty acyl-CoA dehydrogenase activity hereditary disease very long chain acyl-CoA dehydrogenase deficiency https://www.malacards.org/card/acyl_coa_dehydrogenase_very_long_chain_deficiency_of NCIT:C98647 NORD:1827 VLCAD NANDO:2200512 ICD10CM:E71.310 An inherited disorder of mitochondrial long-chain fatty acid oxidation with a variable presentation including: cardiomyopathy, hypoketotic hypoglycemia, liver disease, exercise intolerance and rhabdomyolysis. ACADVLD VLCADD acyl-CoA dehydrogenase, very long-chain deficiency very long chain acyl-CoA dehydrogenase deficiency very long-chain acyl-Coenzyme A dehydrogenase deficiency GARD:0005508 very long-chain acyl-CoA dehydrogenase deficiency icd11.foundation:907810567 VLCAD deficiency UMLS:C3887523 MEDGEN:854382 MONDO:0008723 NANDO:2201139 acyl-CoA dehydrogenase, very long-chain, deficiency OF Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD) DOID:0080155 Orphanet:26793 OMIM:201475 SCTID:237997005 disorder of fatty acid oxidation and ketogenesis familial hypertrophic cardiomyopathy