| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An urea cycle disorder that involves the accumulation of ammonia in the blood. (Human Disease Ontology, DOID_9273) |
| External Link | http://www.omim.org/entry/215700 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the citrullinemia phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ASS1 | argininosuccinate synthase 1 |
