Autosomal recessive hereditary disorder
Disorder of branched-chain amino acid metabolism
Inborn error of metabolism
Specific enzyme deficiency
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Deficiency of hydroxymethylglutaryl-CoA lyase (disorder)
Deficiency of hydroxymethylglutaryl-CoA lyase
HMG-CoA lyase deficiency
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency
deficiëntie van hydroxymethylglutaryl-co-enzym A-lyase
HMG-CoA-lyasedeficiëntie
Id124611007
StatusPrimitive
OccurrenceCongenital
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetE88.0
RuleTRUE
AdviceALWAYS E88.0 | POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE
CorrelationSNOMED CT source code to target map code correlation not specified