|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the Juvenile GM>1< gangliosidosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|GLB1||galactosidase, beta 1|