|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A multiple carboxylase deficiency that involves a deficiency in holocarboxylase synthetase. (Human Disease Ontology, DOID_859)|
|Downloads & Tools|
1 genes associated with the holocarboxylase synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
|HLCS||holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase)|