| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/611945 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the spastic paraplegia 37, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SPG37 | spastic paraplegia 37 (autosomal dominant) |
