Dataset | OMIM Gene-Disease Associations |
Category | disease or phenotype associations |
Type | phenotype |
External Link | http://www.omim.org/entry/612539 |
Similar Terms | |
Downloads & Tools |
1 genes associated with the spastic paraplegia 42, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
Symbol | Name |
---|---|
SLC33A1 | solute carrier family 33 (acetyl-CoA transporter), member 1 |