long chain 3-hydroxyacyl-CoA dehydrogenase deficiency https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/long_chain_3_hydroxyacyl_coa_dehydrogenase_deficiency LCHAD deficiency long-chain 3-OH acyl-CoA dehydrogenase deficiency 3-hydroxyacyl-CoA dehydrogenase long chain deficiency LCHADD OMIM:609016 SCTID:726021008 trifunctional protein deficiency type 1 fatty liver, acute, of pregnancy long chain 3-hydroxyacyl-CoA dehydrogenase deficiency NCIT:C129929 long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency MEDGEN:778253 MONDO:0012173 long-chain 3-hydroxy acyl CoA dehydrogenase deficiency DOID:0061186 Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) is a mitochondrial disorder of long chain fatty acid oxidation characterized in most patients by onset in infancy/ early childhood with hypoketotic hypoglycemia, metabolic acidosis, liver disease, hypotonia and frequently cardiac involvement with arrhythmias and/or cardiomyopathy. UMLS:C3711645 icd11.foundation:760613381 Orphanet:5 HELLP syndrome, maternal, of pregnancy GARD:0006867 disorder of fatty acid oxidation and ketogenesis 3-hydroxyacyl-CoA dehydrogenase deficiency hereditary peripheral neuropathy familial hypertrophic cardiomyopathy obsolete_long chain 3-hydroxyacyl-CoA dehydrogenase deficiency