Mast Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A hereditary spastic paraplegia associated with dementia. (Human Disease Ontology, DOID_0060245)
External Link https://www.disgenet.org/browser/0/1/0/C1855346
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Genes

2 genes associated with the disease Mast Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALDH16A1 aldehyde dehydrogenase 16 family, member A1
SPG21 spastic paraplegia 21 (autosomal recessive, Mast syndrome)