Mast syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A hereditary spastic paraplegia associated with dementia. (Human Disease Ontology, DOID_0060245)
External Link http://www.omim.org/entry/248900
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Genes

1 genes associated with the Mast syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SPG21 spastic paraplegia 21 (autosomal recessive, Mast syndrome)