Spastic paraplegia 42, autosomal dominant Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/612539
Similar Terms
Downloads & Tools

Genes

1 genes associated with the Spastic paraplegia 42, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1