| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An amino acid metabolic disorder that involves the accumulation of argininosuccinic acid (ASA) in the blood and urine. (Human Disease Ontology, DOID_14755) |
| External Link | http://www.omim.org/entry/207900 |
| Similar Terms | |
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1 genes associated with the argininosuccinic aciduria phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ASL | argininosuccinate lyase |