| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | NT MGI. (Human Disease Ontology, DOID_0060269) |
| External Link | http://www.omim.org/entry/612390 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the pontocerebellar hypoplasia type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| TSEN34 | TSEN34 tRNA splicing endonuclease subunit |
