| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | NT MGI. (Human Disease Ontology, DOID_0060278) |
| External Link | http://www.omim.org/entry/615809 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the pontocerebellar hypoplasia, type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| AMPD2 | adenosine monophosphate deaminase 2 |
