Disease #00011 (VLCADD (very long chain acyl-CoA dehydrogenase deficiency), OMIM:609575)

Official abbreviation VLCADD
Name very long chain acyl-CoA dehydrogenase deficiency
OMIM ID 609575
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ACADVL
Associated tissues heart muscle
Disease features -
Remarks -

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