| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An organic acidemia that disrupts or prevents normal metabolism of the branched-chain amino acid leucine. (Human Disease Ontology, DOID_14753) |
| External Link | http://www.omim.org/entry/243500 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the isovaleric acidemia phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| IVD | isovaleryl-CoA dehydrogenase |
