Disease #00009 (MCADD (Medium-chain Acyl-CoA dehydrogenase deficiency), OMIM:607008)

Official abbreviation MCADD
Name Medium-chain Acyl-CoA dehydrogenase deficiency
OMIM ID 607008
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ACADM
Associated tissues liver
Disease features -
Remarks -