Tay-Sachs Disease, AB Variant Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_4795)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D049290
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1 genes/proteins associated with the disease Tay-Sachs Disease, AB Variant from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GM2A GM2 ganglioside activator 2.88009