Very long chain acyl-CoA dehydrogenase deficiency

Disease Export to PDF
Name:
Very long chain acyl-CoA dehydrogenase deficiency
Description:
Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency (VLCADD) is an inherited disorder of mitochondrial long-chain fatty acid oxidation with a variable presentation including: cardiomyopathy, hypoketotic hypoglycemia, liver disease, exercise intolerance and rhabdomyolysis.
ORPHAcode:
26793
Synonyms:
VLCAD deficiency
VLCADD
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14