Juvenile GM>1< gangliosidosis Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description GM1 gangliosidosis type 2 is a clinically variable, infancy or childhood-onset form of GM1 gangliosidosis (see this term) characterized by normal early development and psychomotor regression between seven months and three years of age. (Orphanet Rare Disease Ontology, Orphanet_79256)
External Link http://www.omim.org/entry/230600
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Genes

1 genes associated with the Juvenile GM>1< gangliosidosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
GLB1 galactosidase, beta 1