| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A histidine metabolism disease that involves a deficiency of the enzyme histidase. (Human Disease Ontology, DOID_0060168) |
| External Link | http://www.omim.org/entry/235800 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the [histidinemia] phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| HAL | histidine ammonia-lyase |
