Human genes for GM1 gangliosidosis type 2
GM1 gangliosidosis type 2 [DOID:0080501]
A GM1 gangliosidosis that is characterized by slowly progressive generalized neurodegeneration and mild skeletal changes, with onset between 7 months and 3 years of age.
Synonyms: GM1 gangliosidosis type 2, DOID:0080501, juvenile GM1 gangliosidosis