| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Dystonia 16 (DYT16) is a very rare and newly discovered movement disorder which is characterized by early-onset progressive limb dystonia, laryngeal and oromandibular dystonia, and parkinsonism. (Orphanet Rare Disease Ontology, Orphanet_210571) |
| External Link | http://www.omim.org/entry/612067 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the dystonia 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| PRKRA | protein kinase, interferon-inducible double stranded RNA dependent activator |
